Next Article in Journal
A Perspective on the Comparative Antileukemic Activity of 5-Aza-2′-deoxycytidine (Decitabine) and 5-Azacytidine (Vidaza)
Previous Article in Journal
Role of Transient Receptor Potential Vanilloid 1 in Inflammation and Autoimmune Diseases
Previous Article in Special Issue
Effects of Scrophularia ningpoensis Hemsl. on Inhibition of Proliferation, Apoptosis Induction and NF-κB Signaling of Immortalized and Cancer Cell Lines
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:

Phytomedicine in Otorhinolaryngology and Pulmonology: Clinical Trials with Herbal Remedies

Koosha Ghazi-Moghadam
Hasan Mete Inançlı
Nazanin Bazazy
Peter K. Plinkert
Thomas Efferth
4 and
Serkan Sertel
Department of Otorhinolaryngology, Head & Neck Surgery, University of Heidelberg, Im Neuenheimer Feld 400, 69120 Heidelberg, Germany
Molecular Mechanisms of Head and Neck T—A102, Division Signal Transduction and Growth Control, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120 Heidelberg, Germany
Department of Otorhinolaryngology, Near East University Hospital, 922022 Lefkosa, Turkish Republic of Northern Cyprus
Department of Pharmaceutical Biology, Institute of Pharmacy and Biochemistry, University of Mainz, Staudingerweg 5, 55099 Mainz, Germany
Author to whom correspondence should be addressed.
Pharmaceuticals 2012, 5(8), 853-874;
Submission received: 5 July 2012 / Accepted: 8 August 2012 / Published: 20 August 2012
(This article belongs to the Special Issue Phytomedicine)


Phytomedicine has become an important alternative treatment option for patients in the Western world, as they seek to be treated in a holistic and natural way after an unsatisfactory response to conventional drugs. Ever since herbal remedies have been introduced in the Western world, clinicians have raised concerns over their efficacy and possible side-effects. A PubMed (Medline) search was performed covering the last five years (01/07–04/12) and including 55 prospective clinical randomized control trials in the medical specialities Otorhinolaryngology and Pulmonology. In this review, we present evidence-based clinical data with herbal remedies and try to enlighten the question of efficacy and reliability of phytomedicine.

1. Introduction

Phytomedicine is defined as the use of plants, parts of plants as well as isolated phytochemicals for the prevention and treatment of various health concerns [1]. Medical treatments cover the application of different components of plants (blossom, leaf, stem, radix), aromatic essential oils and herbal extracts as herbal teas, via massage as packs or wraps or in therapies using water, steam or inhalation [2]. Phytomedicine is covered in many traditional medicines, e.g., Traditional Chinese Medicine (TCM) or Kampo Medicine [2,3,4]. Herbal remedies have played an important role in treatment from ancient to modern times. Although these subjects lost their importance in 20th century because of the modern synthetic treatments, there is a renewed interest today in medicinal plants usage as natural products for the generation of semi-synthetic derivatives [2].
Phytomedicine has become an important alternative treatment option for patients in the Western world, as they seek to be treated in a holistic and natural way after an unsatisfactory response to conventional drugs. In fact, patients living in Eastern countries with a long history of traditional medicines regularly use herbal drug prescriptions, as Western medications are hardly affordable for the majority of the population. Ever since herbal remedies have been introduced in the Western world, clinicians have always raised concerns over their efficacy and possible side-effects.
The application of phytomedicines, especially in private practices, is booming. In Western Europe annual revenues reached US$ 5 billion in 2003–2004, while in China sales of products totaled US$ 14 billion in 2005 [5]. This development is founded in patients’ desire to be treated in a holistic and natural way. Moreover, phytomedicines provide valuable resources to meet the requirements for global health care at affordable prices [6]. According to the World Health Organization (WHO), nearly 80% of the population of developing countries, even nowadays, relies on phytomedicines as their only affordable source of medication [7]. The question arises whether this development is justified and can be objectively proven by controlled, randomized clinical trials. Recognition and application of phytomedicine into Western medicine depends most importantly on evidence-based clinical data. In this review, we focus on evidence-based clinical data with herbal remedies in the treatment of diseases in Otorhinolaryngology and Pulmonology.

2. Material and Methods

A PubMed (Medline) search was performed on international publications covering the last five years from January 2007 until April 2012, complying following inclusion and exclusion criteria. The search was limited to the terms “phytomedicine”, “herbal drug”, “herbal medicine”, “natural product”, “natural drug”, “traditional medicine” and frequently used medicinal plants. Inclusion criteria in selecting the publications were set as following: Type of article: clinical trials and randomized controlled trials; Species: humans; Language: English. In addition, clinical trials were selected as to medical branch, scientific quality of study design and clinical impact. As to medical branches, the focus was set on Otorhinolaryngology and Pulmonology. Only prospective, randomized, placebo-controlled, and double-blind designed trials were selected as golden standard of clinical trials.
Exclusion criteria in selecting the publications were phase I studies, case series, and retrospective studies. Supplementary, we performed a proactive Medline search on frequently used medicinal plants
(Ginseng, Echinacea, Salvia, and Ginkgo biloba) in the medical branches mentioned above, which we did not found in our initial search and included interesting publications in this review. In addition, we performed a Medline Search with “phytotherapy” as a Medical Subjects Heading (MeSH) term with the mentioned limits and subsequently checked the references available for each article.

3. Results

3.1. Rhinitis and Sinusitis

Allergic rhinitis is associated with sneezing, nasal discharge, and nasal obstruction. The common therapy strategy of allergic rhinits is usually on avoidance or removal of antigens and symptom therapy with antihistamines and topical steroids, but the potential side-effects of these drugs with long-term usage are of concern. Patients have demanded alternative therapy options, especially with traditional and herbal medicine. In Table 1 various herbal remedies in the treatment of allergic rhinitis and acute rhinosinusitis are listed.
Naringenin chalcone as the effective constituent of tomato extracts has been shown to inhibit the release of histamine from mast cells in the initial phase of inflammation and decrease the eosinophils and eosinophil cationic proteins. In a randomized double blind study from Japan, the effects of tomato( Lycopersicon esculentum Miller) extracts (TE, 360 mg per day for eight weeks) on patients with mild to moderate perennial allergic rhinitis were studied. In the TE group, nasal obstruction, rhinorrhea, and sneezing were improved significantly compared to placebo (p < 0.05) [8].
In another study, a combined herbal therapy (ARND) against perennial allergic rhinitis was tested in a randomized, double-blinded and placebo-controlled setting, with a crossover arrangement for the administration of allergic rhinitis nasal drop or placebo. ARND consisted of Herba centipedae 23%, Herba menthae 16%, Radix paeoniae alba 16%, Radix scutellariae 10%, Radix glycyrrhizae 6%, Radix platcodi 6%, Flos lonicerae 5%, Fructus zizyphi jujubae 5%, Rhizoma coptidis 4%, Radix ledebouriellae 5%, and Pericarpium citri reticulatae 4%. Each of these herbal remedies has anti-bacterial and anti-inflammatory activity. ARND relieved clinical symptoms in patients with perennial allergic rhinitis and improved their quality of life [9].
Effects of another combined herbal therapy against allergic rhinitis were studied in a randomized, double-blinded crossover trial. The herbal tablet consisting of Cinnamomum zeylanicum, Malphighia glabra and Bidens pilosa were compared to the positive control treatment with loratadine and placebo. The herbal tablet significantly reduced nasal symptoms and inhibited the release of prostaglandin D2 in nasal lavage analysis [10].
Shi-Bi-Lin (SBL) a herbal remedy consisting of 7.5 g Xanthium sibiricum Patrin ex Widder (Fructus asteraceae), 20 g Angelica dahurica (Fisch. ex Hoffm.) Benth. (Radix apiaceae), 7.5 g Saposhnikovia divaricata (Turcz.) Schischk. (Radix apiaceae), 15 g Magnolia biondii Pamp. (Flos magnoliae), 5 g Gentiana scabra Bunge (Radix gentianaceae) and 5 g Verbena officinalis L. (Herba verbenaceae) has been shown to suppress eosinophil infiltration in animals’ nasal tissues and inhibited the expression of endothelial nitric oxide synthase and release of thromboxane B2, which are playing an important role in the acute phase of inflammation [11]. In a randomized, double-blinded, placebo-controlled study, there were no significant improvements in the symptoms of patients with perennial allergic rhinitis treated with SBL in comparison to placebo as control for a limited period of 4 weeks [12].
Dust mite allergy is one of the most common reasons for allergic rhinitis. Ten-cha (Rubus suavissimus) represents a common phytotherapeutic against allergic rhinitis in Japan. In a randomized, double-blinded, placebo-controlled study ten-cha (with dosage of 400 mg three times per day) could improve nasal symptoms without showing significant differences to the placebo [13]. In another study from Croatia, Matkovic et al. investigated the effect of Astragalus membranaceus (AM), a herbal remedy with immunomodulatory characteristics. In their double-blinded, placebo-controlled clinical trial AM significantly decreased the intensity of rhinorrhea without any significant changes in IgE level and eosinophil counts in patients in comparison to placebo [14].
Nigella sativa, a plant mostly used in traditional medicine in the Middle East and Mediterranean area, has been described with anti-inflammatory and anti-allergic effects through changes in activity of phagocytosis and killing activity of polymorphonuclear (PMN) leucocytes, leukotriene synthesis, and inhibition of histamine release [15]. Its effect on patients with allergic rhinitis has been investigated in two studies. Nigella sativa seeds have been shown to significantly increase phagocytosis and killing activity of PMNs and count of T-cell receptors in patients after immunotherapy rather than patients receiving conventional immunotherapy [16]. In another study, patients treated with Nigella sativa oil for 30 days had significant improvements of nasal signs and symptoms [17].
Idiopathic rhinitis (IR), as one differential diagnosis to perennial rhinitis, is an impairment of nasal breathing accompanied by sneezing, nasal itching, and rhinorrhoea. Dysregulation in the neurogenic mechanism of blood supply to the cavernous tissue of the inferior turbinate is discussed as the major pathomechanism of IR [18,19]. Neuropeptides like substance P from the sensory neurons of nasal mucosa are claimed to play a major role in the neurogenic mechanism of IR. Capsaicin, the active component of plants belonging to the genus Capsicum, interacts with sensory neurons [20]. Intranasal application of Capsicum spray in IR was evaluated in a randomized placebo-controlled trial. Capsicum (4 mg/puff, three times a day for three consecutive days) showed a significant reduction in the frequency of IR symptoms compared to controls [21].
Acute rhinosinusitis is one of the most frequently treated diseases in Otorhinolaryngology. A root extract of Pelargonium sidoides, originating from South Africa and traditionally used as a medicinal plant by the Zulu, is used in Europe against acute bronchitis, tonsillopharyngitis, and common cold [22,23]. In a randomized, double-blinded, placebo-controlled trial Pelargonium sidoides (Umckaloabo) extract EPs® 7630 influenced the course of acute rhinosinusitis favourably and caused a faster recovery compared to placebo [24]. Pelargonium sidoides has been described as an immune stimulant, inhibitor of bacterial adhesion to mucus and also multiplier of cilliary beat frequency [25]. In a randomized, double-blinded study, treatment with a dosage of 30 drops three times a day with Pelargonium sidoides, yielded an improvement of sinus severity scores after seven days [24]. However, Umckaloabo is suspected of being hepatotoxic [26]. Eucalyptus oil is one of the most famous phytomedicines used by patients and physicians against acute rhinosinusitis. The main constituent of eucalyptus oil is cineole. Its efficacy and safety against acute rhinosinusitis were proven in a placebo-controlled, double-blinded and randomized clinical trial [27]. Remarkably, treatment of purulent rhinosinusitis with cineole reduced symptoms more effectively and statistically significant compared to an alternative herbal preparation composed of five different medicinal plants (12 mg Gentianae radix, 36 mg Primulae flos cum calycibus, 36 mg Ramicis herba, 36 mg Sambuci flos, and 36 mg Verbenae herba) [28]. In this case, cineole as the main constituent of eucalyptus is seen clinically as superior to a combination of medicinal herbs, which are supposed to be effective against acute rhinosinusitis. This represents an exception as therapeutic efficacy of phytomedicine is based on synergistic or antagonistic interaction of many phytochemicals [7].

3.2. Olfactory Loss

Olfactory loss happens to be a complication after acute and chronic sinusitis due to viral infections. Swelling of the olfactory cleft after infection and degeneration of neurosensoral function are mentioned as its pathgenesis. Ginkgo biloba has been attributed to olfactory regeneration in animal models. In a well-designed, double-blinded, controlled trial a combination therapy of Ginkgo biloba with mometasone nasal spray was compared to mometasone monotherapy in patients with postviral olfactory loss. The results show significant improvements of odor threshold and identification in the combination therapy group [29].

3.3. Asthma

Asthma is defined as a recurrent and reversible obstruction of the respiratory tract with bronchospasm, cough, wheezing, and dyspnea. Avoidance of allergens and the application of inhalative sympathomimetics, oral or inhalative corticosteroids, and leukotriene antagonists are the main therapeutic lines. Here, we focus on phytomedicines with clinical evidences in the treatment of asthma (Table 2).
Nigella sativa has been found as a histamine antagonist and inhibitor of the histamine receptor. It is certified as anti-inflammatory, anti-tussive and anti-cholinergic as well. A placebo-controlled trial has shown that treatment of asthmatic patients with an extract of Nigella sativa for three months improved symptoms and pulmonary function tests [30]. French maritime pine bark is well-known for its anti-inflammatory effect via inhibition of 5-lipooxygenase expression. It has been proven that its anti-asthmatic effects could be boostered when patients use inhalative corticosteroids as a basic therapy. In a well-designed study, the extract of this herbal remedy was administered in form of oral tablets in patients with allergic asthma. In a six-months therapy, significant improvements in asthma signs and symptoms together with a reduced need of conventional asthmatic medications could be seen [31]. Similar results yielded with the use of Sophora flavescens in patients with refractory chronic asthma [32]. This herbal remedy proved to have anti-asthmatic characteristics in mast cell derived allergic inflammation diseases [33]. Purple passion fruit peel extract has been attributed to inhibit histamine release and involve in arachidonic acid metabolism. In a randomized, double-blinded study, effects of this herbal plant with dosage of 150 mg daily for four weeks treatment were compared to placebo; it has been shown that asthma symptoms like cough, wheezing, dyspnea, and force vital capacity (FVC) were significanty improved. However, forced expiratory volume in one second (FEV1) had no significant difference [34]. Two clinical trials studied the effects of combined formulas on asthmatic patients. In a crossover, randomized control study, effects of an oral treatment with a combined formula (Picrorrhiza kurroa, apocynin, Picrorrhiza kurroa and Zingiber officinale) and a standardized extract of Ginkgo biloba were investigated on therapy-refractory asthmatic patients. No significant improvements in asthma symptoms, pulmonary function test (PFT), and quality of life could be seen [35]. Another study with a herbal remedy (Astragalus mongholius Bunge, Cordyceps sinensis Sacc., Radix stemonae, Bulbus fritillariae cirrhosae, and Radix scutellariae) was performed in pediatric asthma patients for six months with no improvement in lung function tests and other biometrical parameters [36].

3.4. Respiratory Tract Infection

Although upper respiratory tract infections are the most common infections in general population, lower respiratory tract infections are the leading cause of death among infectious diseases [37]. As phytomedicines have antibacterial, antiviral or immune modulatory effects, there are clinical evidences for the prevention and treatment of respiratory tract infections (Table 3).
Pelargonium sidoides extracts are widely used in the treatment of respiratory tract infections, e.g., acute rhinosinusitis and bronchitis. Its antimicrobial and anti-inflammatory characteristics are based on the release of tumor necrosis factor α (TNFα), nitric oxide, and increase in natural killer cells activity [38]. With the therapeutic dosage of 30 drops three times per day for at least seven days, patients show significant improvements in symptoms of common cold and acute bronchitis [23,39,40]. This is in accordance with a double-blind dose-finding study in which patients with acute bronchitis were treated with different dosages of Pelargonium sidoides extracts (tablet 10, 20, and 30 mg three times per day). The therapeutic results of these three treatment groups were superior to placebo with an optimal dose of 20 mg three times per day in consideration of the benefit risk ratio [41]. Thyme and primrose root are attributed with antibacterial, anti-fungal, and mucolytic characteristics. Patients treated with a combination of thyme and primrose root showed a significant reduction of cough, severity, and duration of acute bronchitis [42]. Ivy leaves extract represents another common medicinal plant used in the treatment of bronchitis due to its proven anti-inflammation, anti-congestion, antibacterial, and antispasmodic characteristics. A seven days oral treatment with ivy leaves extract reduced severity, and symptoms of acute or chronic bronchitis [43]. This accords with another study, in which two forms of ivy leaves extracts (Hedelix® and Prospan®) significantly reduced severity of bronchitis compared to placebo [44]. Although adverse effects of ivy leaves extracts are low (2% of patients), it was indicated that the risk of occurance of side-effects could rise in concomitant therapy with antibiotics up to 26% of cases [43].
Echinacea has always been known to activate the immune system and anti-inflammatory reactions through the up-regulation of TNFα [45,46]. Therapeutic effects of Echinacea extract on sore throat and tonsillitis were investigated in two studies. In a double-dummy controlled trial, effects of Echinacea spray in combination with sage were compared to chlorohexidin/lidocain combination on sore throat. Interestingly, 60% of patients in each group became symptom-free after three days with no significant difference between these two combinations [47]. A Japanese herbal combination (Gypsum, Radix bupleuri, Tuber pinelliae, Radix scutellariae, Radix platycodi, Fructus jujube, Radix panacis ginseng, Radix glycyrrhizae, and Rhizoma zingiberis) was shown to be effective in chronic and recurrent tonillitis. After one year of treatment, the incidence of acute tonsillitis in patients with chronic tonsillitis decreased in seven of ten cases [48].
Table 1. Herbal remedies in the treatment of allergic rhinitis and acute rhinosinusitis.
Table 1. Herbal remedies in the treatment of allergic rhinitis and acute rhinosinusitis.
YearAuthorDiseaseHerbal remedyPatientEffectsDosage
2007YoshimuraAllergic rhinitisnaringenin chalcon/tomato extracts33Inhibition of histamine release frommast cells360 mg/oral/8 weeks
2008CorrenAllergic rhinitisCinnamomum zeylanicum, Malphighia glabra, Bidens pilosa20Inhibition of neutrophil migration and mast cell production, reduction of histamine concentration2 capsules/3 times per day/3 days
2008TescheAcute viral rhinosinusitisCineole150Anti-inflammatory, accelerating the beat frequency of cilia and antimicrobial effects200 mg/3 times per day/7 days
2009BachertAcute rhinosinusitisPelargonium sidoides103Immune stimulant, inhibits bacterial adhesion to epithelial cells, stimulates cilliary beat frequency60 drops/3 times per day/for maximum 22 days
2009CiabattiAllergic rhinitisCapsicum oleous 208Activates/desensitizes sensory neurons or peptidergic nerve fibers 4 mg/puff, 3 times per day/3 days
2009ZhaoAllergic rhinitisShi Bi Lin *126Suppression of eosinophil’s’ infiltration in the animals’ nasal tissues, decreasing of endothelial nitric oxide expression, inhibition of thromboxane B2 release500 mg/2 times per day/14 days
2010ChuiAllergic rhinitisARND **35Antibacterial , anti-inflammatory2 sprays/3 times per day/7 weeks
2010IsikAllergic rhinitisNigella sativa24Increase in activity of phagocytosis and intracellular killing activity of PMNs, CD 8 counts, leukotriene synthesis and inhibition of histamine release 2 g oral per day/30 days
2010MatkovicAllergic rhinitisAstragalus membranaceus48Decrease of INF-α, IL-5 and IL-13 80 mg capsules/1 per day/3 weeks
2011NikakhlaghAllergic rhinitisNigella sativa66Increase of phagocytosis, intracellular killing activity of PMNs, CD 8 counts and leukotriene synthesis, inhibition of histamine release2 g oral per day/30 days
2011YonekuraAllergic rhinitisRubus suavissimus (ten cha)87Anti-inflammatory effects, inhibits releasing of histamine from mast cells400 mg capsule/3 times per day/4 weeks
*: 7.5 g Xanthium sibiricum Patrin ex Widder (Fructus asteraceae), 20 g Angelica dahurica (Fisch. ex Hoffm.) Benth. (Radix apiaceae), 7.5 g Saposhnikovia divaricata (Turcz.) Schischk. (Radix apiaceae), 15 g Magnolia biondii Pamp. (Flos magnoliae), 5 g Gentiana scabra Bunge (Radix gentianaceae) and 5 g Verbena officinalis L. (Herba verbenaceae). **: Herba centipedae 23%, Herba menthae 16%, Radix paeoniae alba 16%, Radix scutellariae 10%, Radix glycyrrhizae 6%, Radix platcodi 6%, Flos lonicerae 5%, Fructus zizyphi jujubae 5%, Rhizoma coptidis 4%, Radix ledebouriellae 5%, and Pericarpium citri reticulatae 4%.
Table 2. Herbal remedies in the treatment of asthma.
Table 2. Herbal remedies in the treatment of asthma.
YearAuthorHerbal remedyPatientEffectsDosage
2007BoskabadyNigella sativa29Relaxant, anticholinergic, antihistaminic375 mL/kg 50% boiled extract for 2 months
2007HoangSophora flavescens14Anti-inflammatory activity, anti-asthmatic effect4 g/2 times per day/3 months
2007ThomasAKL 1 *32Antibacterial, antioxidant, immunomodulatory, anti-inflammatory, anti-bronchospasm500 mg/2 times per day/12 weeks
2008Watsonpurple passion fruit peel-Antioxidant, antiallergic, anti-inflammatory, decreasing of nitric oxide150 mg/daily/4 weeks
2009WongCombination of botanical product **85Antibacterial, antitussive, anti-inflammation0.619 g capsule/daily/6 months
2011BelcaroFrench maritime pine bark extract (Pycnogenol)76Antioxidant, anti-inflammatory, vasodilatation50 mg/2 times per day/6 months
*: Picrorrhiza kurroa, apocynin, Zingiber officinale, a standardized extract of Ginkgo biloba. **: Astragalus mongholius Bunge, Cordyceps sinensis Sacc., Radix stemonae, Bulbus fritillariae cirrhosae and Radix scutellariae.
Table 3. Herbal remedies in the treatment of upper and lower respiratory tract infections.
Table 3. Herbal remedies in the treatment of upper and lower respiratory tract infections.
YearAuthorDiseasePatientHerbal remedyEffectsDosage
2007LizogubCommon cold103Pelargonium sidoides Release of TNFα and nitric oxide, increasing the activities of natural killer cells30 drops/3 times per day/10 days
2007KemmerichAcute bronchitis361thyme herb/primrose rootAntibacterial, antifungal, mucolytic, antitussive1 tab/3 times per day/11 days
2007SchulzAcute bronchitis124Pelargonium sidoidesRelease of TNFα and nitric oxide, increasing the activities of natural killer cells30 drops/3 times per day/7 days
2007MatthysAcute bronchitis217Pelargonium sidoidesRelease of TNFα and nitric oxide, increasing the activities of natural killer cells30 drops/3 times per day/7 days
2007KuboInfluenza 60Mao-ToAntipyretic0.06 g/kg body/3 times per day
2008VohraPediatric upper respiratory tract infections46GinsengImmunomodulatory, release of IL2, TNFα, IL 6, NO600 mg and 400 mg/3 times per day/3 days
2009FazioAcute and chronic bronchitis9,657Ivy leaf (Hedera helix)Anti-inflammatory, anti-congestive, antibacterial, antispasmodic3 times per day/7 days
2009SchapowalSore throat Echinacea/SalviaEchinacea: anti-inflammatory, immune modulatory, upregulation of TNFα, antiviral and antibacterial, Salvia: anti-inflammatory, antibacterial, antinociceptive2 puffs every 2 h
2010BarrettCommon cold713EchinaceaAnti-inflammatory, immune modulatory, antiviral and antibacterial1 tab/2 times per day/14 days
2010MatthysAcute bronchitis Pelargonium sidoidesRelease of TNFα and nitric oxide, increasing the activities of natural killer cellstab 20 mg/1 or 2 or 3 times per day/7 days
2010GotoChronic tonsillitis Sho-saiko-to-ka-kikyo-sekko *Not available daily/12 months
2010KalusUpper respiratory tract infections300Cistus incanus and Green TeaAnti-inflammatory, antibacterial, antifungal and antispasmodic12 tab/daily/7 days
2010SexanaUpper respiratory tract infections223Andrographis paniculata Antibacterial, anti-inflammatory, immune stimulant, antipyretic 200 mg/day/5 days
2010WangInfluenza480Antiwei **Antipyretic, antitussive6g/BID/3 days
2011RollCommon cold529Juice powder concentrate of fruits and vegetablesincrease in plasma levels of antioxidants and T-cells4 capsules daily/8 months
2011CwientzekaAcute bronchitis590Ivy leafAnti-inflammatory, anti-congestive, antibacterial, antispasmodic, sympatomimetic, secretion of surfactant 3 times per day/7 days
*: Gypsum, Radix bupleuri, Tuber pinelliae, Radix scutellariae, Radix platycodi, Fructus jujube, Radix panacis ginseng, Radix glycyrrhizae and Rhizoma zingiberis. **: Mahuang (Herba Ephedra), Baimaogeng (Rhizoma Imperatae), Gegen (Radix puerariae), Guizhi (Ramulus Cinnamoumum), Kuxingren (Semen Armeniacae Amarum.), Ganjiang (Rhizoma Zingiberis), Gancao (Radix Glycyrrhizae).
The therapeutic effect of Echinacea on acute viral respiratory infection (common cold) was studied with two species (E. purpurea and E. angustifolia). Echinacea tablets containing the equivalent of 675 mg E. purpurea root and 600 mg E. angustifolia root did not yield statistically significant shorter illness duration and lower severity. The authors trace this inefficiency back to the dose of the Echinacea formulation [49]. Preventive effects of a dietary supplement composed of a concentrated mixture of fruits and vegetables (Juice plus) on common cold were investigated in another study. This product contains antioxidants like vitamin B and C or β-carotene and is an immunomodulatory agent. Eight months administration of Juice plus could reduce the severity and duration of common cold [50]. Camellia sinensis has also a preventive role in flu and common cold in healthy patients. It can increase the interferon release and proliferation of T cells challenged in vitro [51].
A double dummy controlled trial compared the effects of Mao-to and oseltamivir as an antipyretic agent in Influenza typ A. This remedy is known as an immune modulator and stimulates the release of interferon β from host cells. In this study, patients were categorized in three groups (oseltamivir alone, Mao-to alone and combined therapy of these two). Mao-to powder alone or as a combination with oseltamivir tablets could reduce fever in patients significantly [52]. A three-day treatment with Antiwei tablets, a herbal mixture (see Table 3), has indicated to be significantly effective on severity and duration of Influenza in comparison to placebo. This mixture in tablet form has antipyretic and antitussive effects [53].
Green tea has antibacterial, antitoxic, antiviral, and antifungal activities in upper and lower respiratory tract infections [54]. In the same manner, Cistus incanus extract (CYSTUS052) has also shown antibacterial, antiviral, anti-inflammatory, and antispasmodic effects in different diseases. Cistus incanus has been indicated to have a better effect on duration and severity in viral and bacterial infections of the upper respiratory tract compared to green tea [55]. Ginseng stimulates the immune system and enhances the production of interleukin 2, TNFα, interlukeukin 6, nitric oxide in murine spleen cells [56]. In a control trial study in order to determine safety and dosage of ginseng, children with upper respiratory tract infections were treated in three arms with different ginseng dosages. The standard dose (600 mg TID day 1, 400 mg TID day 2 and 200 mg TID day 3) and half of the standard dose of ginseng were compared to a placebo group. Frequency and severity of respiratory tract infections and reported adverse events were not significantly different among these three arms [57]. In contrast, Andrographis paniculata tablets (200 mg/day) in a 5-day treatment were superior to placebo in the treatment of upper respiratory tract infection syndroms [58].

3.5. Chronic Obstructive Pulmonary Disease (COPD)

Chronic inflammation, related respiratory tract stenosis and impaired mucocilliary movements in chronic obstructive pulmonary disease (COPD) lead to dyspnea, chronic cough with sputum and impaired pulmonary function tests. COPD patients can be treated with antibiotics, bronchodilators, and corticosteroids [59].
Hochuekkito, containing ten Japanese herbs, has been known to have anti-inflammatory effects. In a six-months study, with the dosage of 2.5 mg tablets three times per day plus bronchodilators as a basic treatment in elderly patients with COPD, patients had better FEV1, TNFα and c-reactive protein blood and interleukin 6 level in comparison to the placebo group [60]. Echinacea purpurea (EP) is known as an immune modulator and can help in induction of apoptosis, cell migration and inhibition of TNFα. The effect of EP, placebo and EP plus micro-nutritions (zinc, selenium and Vitamin C) were compared with each other for seven days [61]. Since only the EP+ group had better results than placebo, it seems that in a short time, the effect of this herbal remedy could be boosted in accompanying with micro-nutritions [62].
Since cineole has positive effects on the beat frequency of the cilia and bronchodilation, it may show positive influence on the exacerbations of COPD and lung function tests [27,63]. Patients who received 200 mg of cineole tablets three times a day had a reduction of exacerbations such as dyspnea and improvements of lung function and health status [64].

3.6. Otitis Media

Recurrent otitis media in young children has been tried to treat with Echinacea in combination with osteopathic manipulative treatment (OMT). For this purpose, an American group of pediatricians conducted a randomized, placebo-controlled trial with a six-month follow-up over four years. Children aged 12–60 months with recurrent otitis media received an alcohol extract of Echinacea purpurea roots and seeds (or placebo) for ten days at the first sign of common cold. Five OMT visits (or sham treatments) were offered over three months. Remarkably, Echinacea purpurea was associated with a borderline increased risk of having at least one episode of acute otitis media during six-months follow-up compared to placebo, whereas no interaction was found between Echinacea and OMT [65].

3.7. Ideopatic Hearing Loss and Tinnitus

Ideopathic sudden hearing loss and tinnitus aurium represent diseases frequently treated in Otorhinolaryngology. Pentoxifylline and cortisone represent long-established drugs against sudden hearing loss and acute tinnitus. Although there is a lack of definitive evidence-based data, they are still in clinical use. This dillema promotes the trying of complementary and alternative medicine. Ginkgo biloba represents one of the most used phytomedicines in Otorhinolaryngology against sudden hearing loss and tinnitus. The efficacy of ginkgo special extract EGb 761 in patients with chronic tinnitus was studied. In this trial, patients received a 10 days intravenous treatment with 200 mg/day EGb 761, after they were randomized to a double-blind oral treatment with either 2 × 80 mg/day EGb 761 or placebo with a treatment period of 12 weeks. Interestingly, the combination of intravenous followed by oral treatment with ginkgo special extract EGb 761 appeared to be effective and safe in reducing the individual sound intensity of tinnitus [66]. In another trial, EGb 761 was compared to a conventional treatment with pentoxifylline for sudden hearing loss. Treatment with EGb 761 was as effective as treatment with pentoxifylline [67]. In a multicentre, randomized, double-blind phase III study, administered oral doses of 120 mg twice daily and 12 mg twice daily over eight weeks were compared. It is reported that the higher dose of EGb 761 appears to accelerate the recovery of patients with sudden hearing loss less than 75 dB, with a good chance of complete recovery [68].
A treatment combination of aescin and troxerutin against hearing loss caused an improvement in the hearing level (>10 dB) of patients in contrast to pentoxyfylline [69]. It has shown that aescin can induce endothelial nitric oxide synthesis and is an angatonist of serotonin and histamine. These effects can help in treating inflammation, fluid collection, and thereby improve the sound conduction process [70].

3.8. Oral Cavity

The Eucalyptus globulus leave is reported to have antibacterial activity against oral bacteria, such as Streptococcus mutans [71]. Eucalyptus extracts in chewing gum has been shown to significantly inhibit plaque formation, inflammation, and bleeding of gingiva [72]. Streptococcus mutans activity can also be inhibited by Terminalia chebula as it increases the pH-value of saliva [73].
Leaves of myrtle (Myrtus communis) have been attributed with antibacterial, analgesic, anti-inflammatory, and free-radical scavenging activities. In a controlled trial, the application of a paste containing 5% myrtle was effective in the treatment of recurrent aphtus stomatitis. It could significantly reduce ulcer size, pain severity, erythema, and exudation level of recurrent aphthous stomatitis [74]. Rosa damascene is known to have antibacterial, antioxidant, antitussive, hypnotic, and antidiabetic effects. The results of one study showed that a mouthrinse containing Rosa damascena extract was more effective although not more significant than the placebo in severity of pain, size, and number of the ulcers of recurrent aphthous stomatitis [75].

3.9. Oncology

Chinese herbal recipe, “Feiji Recipe” was reported to improve clinical symptoms of middle stage and advanced non-small cell lung cancer (NSCLC). The remedy decoction consists of: Radix astragali 30 g, Radix glehniae 15 g, Tuber ophiopogonis japonici 12 g, Tuber asparagi cochinchinenses 12 g, Sclerotium poriae cocos 15 g, Selaginelladoed 30 g, Salvia chinensia 30 g, Herba cum radice houttuyniae cordatae 30 g and Houttuynia cordata 24 g. In a randomized, controlled pilot study, simultaneous application of “Feiji Recipe” and chemotherapy in patients with NSCLC could prevent the worsening of function in terms of role, social, fatigue, and global health evaluated with the Core Quality of Life Questionnaire (QLQ-C30) [76].
Green tea is attributed to various healthy benefits, e.g., prevention of cardiovascular diseases and cancer in preclinical studies [77]. From the M.D. Anderson Cancer Center in Houston comes a phase II randomized, placebo-controlled trial with green tea extract (GTE) in patients with high-risk oral premalignant lesions. Patients receiving high doses of green tea extract GTE (750 and 1,000 mg/m2) three times daily for 12 weeks showed clinical response and improvements of histology [78]. GTE contains high amounts of polyphenols, including epigallocatechin 3-gallate (EGCG) and could prevent oral cancer in preclinical models [79]. EGCG regulates apoptosis and blocks angiogenesis by decreasing phosphorylation of vascular endothelial growth factor receptor and inhibits its release from tumor cells [80].
Rhubarb has been well-known in Chinese medicine for its medical properties. In a recent study, rhubarb extract significantly attenuated radiation, induced lung toxicity, and improved pulmonary function. This prophylactic effect of rhubarb on lung cancer patients treated with radiotherapy has been explained by decreasing the level of transforming growth factor-beta-1 and interleukin-6 [81].

3.10. Post-Operative Management

Herbal remedies can change the pain score in post-operative patients. Arnica montana has been found to have analgesic effects [82]. Arnica montana extract administered to patients after tonsillectomy significantly decreased their pain scores compared to the placebo group. However, significant changes in analgesic consumption were not noted [83]. In another post-operative study, Melilotus extract has been used in the treatment of ecchymosis after rhinoplasty and blepharoplasty. It could decrease ecchymosis and paranasal, upper, and lower eyelids edema compared with the control group [84].

4. Discussion

Phytomedicine has become an important alternative treatment option in the western world [8,85]. Huge financial, natural and human resources have been spent in this field. The question arises whether this development is justified and can be objectively proven. More than ever before, western physicians demand clinical evidence for the efficacy of phytomedicines in appropriately designed clinical trials. In overview of all publications, there is a need in clarifying whether phytomedical agents could substitute a classical therapy considering efficiency and side-effects. In addition, it would be reasonable to compare effects of herbal remedies with placebo and double dummies. We found four studies with a double dummy design [10,47,52,69]. Furthermore, there is a lack of dose-finding studies. In fact, only two studies evaluated the dosage of phytotherapeutics in patients over the last five years [10,41].
Measurement tools are a very important concern in evaluating the efficiency of therapeutic means. Among the studies reviewed, 27.2% were evaluated subjectively, e.g., quality of life questionnaires or visual analogue scales. Only 16.3% of studies were evaluated with objective measurement tools, e.g., cell counts and function tests. Interestingly, a significant percentage of studies (56.3%) applied both, subjective and objective measurement tools.
Remedies in studies were applied as single or combinations of several phytotherapeutics, e.g., in the form of decoctions. In the latter case, it is difficult to determine the degree of therapeutical contribution of each component. Pharmacological effects are considered to be the result of the synergistic or antagonistic interaction of many phytochemicals [7]. However, it has been shown that a single herbal compound can have a less pharmacological effect than a combination of compounds [28]. In this review, 20% of study results were non-significant with combinations of medicinal plants versus 10% with single herbs.
Evidently, there are several weak and recurrent aspects in the majority of publications in PubMed. Among these are short duration of treatment periods, small sample sizes, inappropriate randomization, blinding, and controls. Application of unknown effective dosages, ignorance of underlying diseases, and patients’ age may also have negative influence on therapeutical efficacy, and statistical power [86]. Moreover, we experienced in our Medline search that a critical number of publications from China are not written in English and/or are not provided with abstracts. Considering the time period from January 2007 until April 2012 with our inclusion criteria and with all available languages, Medline search yielded 1,183 articles covering 322 non-English written publications. Among those, 280 articles were published in Chinese language. Although titles of studies promise to be of clinical interest, further information, and results of individual trials are not provided except for the Chinese-speaking peer-reviewing community. This represents one of various major obstacles in achieving recognition of phytomedicine in western science. Clinical and scientific development can only be assured if experiences are worldwide published in English.
Depending on the chemical contents of each herb, the method of extraction, and also the season of its harvest, efficiency reports of herbal remedies are sometimes inconsistent [57,87]. Another neglected aspect for controversial results in clinical trials is the ignorance of quality control. Quality control comprises the correct identification and authentication of medicinal plants. Moreover, quality control ensures not only proper composition of herbal remedies but also prevents contamination of herbal drugs with mycotoxins, pesticides, heavy metals, and chemical toxins with advanced techniques, e.g., high-performance liquid chromatography fingerprints and random amplified polymorphic DNA analysis [6]. Qualitive and quantitive heterogeneity of production might be a restrictive factor in the clinical evaluation of herbal remedies [88] and represent an important factor of safety for patients. Reports of toxicity vary on available medical guidelines and recommended doses in each country [57,89]. A stepwise evaluation of phytomedical products in phase I to phase III trials, as it is routinely done in pharmaceutical research, would help to clarify this issue.
It must be emphasized that efficacy and safety of phytotherapeutics depend on the quality of phytomedical products. Appropriate quality assurance and control of herbal drugs as well as sustainable production methods are pre-conditions for the implementation of phytomedicine in cancer therapy at an international level [90]. Another neglected aspect for controversial results in clinical trials is the ignorance of quality control. Quality control comprises the correct identification and authentication of medicinal plants. Moreover, quality control ensures not only proper composition of herbal remedies but also prevents contamination of herbal drugs with mycotoxins, pesticides, heavy metals, and chemical toxins with advanced techniques, e.g., high-performance liquid chromatography fingerprints and random amplified polymorphic DNA analysis [6].

5. Conclusions

Phytomedicine is founded on millenia-old knowledge of medicinal plants. Today, it has become a segment of the Asian and even European pharmaceutical market. We have existing and convincing evidence-based clinical data in international databases, e.g., PubMed (Medline). However, recognition and application of phytomedicine into western medicine will depend on credible evidence-based clinical data. Phytomedicine will only enter in professional clinical application if safety, efficacy and quality are proven in a comparable manner to conventional drugs. For this purpose, it is mandatory to conduct well-designed clinical trials. Awareness of Good Clinical Trial Practice and provision of knowledge worldwide is the existential foundation for proper scientific development.

Conflict of Interest

The authors declare no conflict of interest.


  1. Jonas, W.B. Mosby’s Dictionary of Complementary and Alternative Medicine; Elsevier Mosby: St. Louis, MO, USA, 2005; p. 519. [Google Scholar]
  2. Efferth, T.; Li, P.C.; Konkimalla, V.S.; Kaina, B. From traditional chinese medicine to rational cancer therapy. Trends Mol. Med. 2007, 13, 35–61. [Google Scholar]
  3. Efferth, T.; Fu, Y.J.; Zu, Y.G.; Schwarz, G.; Konkimalla, V.S.; Wink, M. Molecular target-guided tumor therapy with natural products derived from traditional chinese medicine. Curr. Med. Chem. 2007, 14, 2024–2032. [Google Scholar] [CrossRef]
  4. Efferth, T.; Miyachi, H.; Bartsch, H. Pharmacogenomics of a traditional japanese herbal medicine (kampo) for cancer therapy. Cancer Genomics Proteomics 2007, 4, 81–91. [Google Scholar]
  5. WHO. Available online: http://www.Who.Int/mediacentre/factsheets/fs134/en/ (accessed on 23 July 2011).
  6. Efferth, T. Perspectives for globalized natural medicines. Chin. J. Nat. Med. 2011, 9, 1–6. [Google Scholar]
  7. Efferth, T.; Koch, E. Complex interactions between phytochemicals. The multi-target therapeutic concept of phytotherapy. Curr. Drug Targets 2011, 12, 122–132. [Google Scholar] [CrossRef]
  8. Yoshimura, M.; Enomoto, T.; Dake, Y.; Okuno, Y.; Ikeda, H.; Cheng, L.; Obata, A. An evaluation of the clinical efficacy of tomato extract for perennial allergic rhinitis. Allergol. Int. 2007, 56, 225–230. [Google Scholar] [CrossRef]
  9. Chui, S.H.; Shek, S.L.; Fong, M.Y.; Szeto, Y.T.; Chan, K. A panel study to evaluate quality of life assessments in patients suffering from allergic rhinitis after treatment with a chinese herbal nasal drop. Phytother. Res. 2010, 24, 609–613. [Google Scholar]
  10. Corren, J.; Lemay, M.; Lin, Y.; Rozga, L.; Randolph, R.K. Clinical and biochemical effects of a combination botanical product (clearguard) for allergy: A pilot randomized double-blind placebo-controlled trial. Nutr. J. 2008, 7, 20. [Google Scholar] [CrossRef]
  11. Zhao, Y.; Leung, P.C.; Woo, K.S.; Chen, G.G.; Wong, Y.O.; Wang, L.H. The effect and therapeutic mechanism of a chinese herbal formula shu-bi-lin (sbl) in the treatment of allergic rhinitis-animal study and in vitro study. J. Allergy Clin. Immunol. 2005, 115, 139. [Google Scholar] [CrossRef]
  12. Zhao, Y.; Woo, K.S.; Ma, K.H.; van Hansselt, C.A.; Wong, K.C.; Cheng, K.F.; Lam, C.W.; Leung, P.C. Treatment of perennial allergic rhinitis using shi-bi-lin, a chinese herbal formula. J. Ethnopharmacol. 2009, 122, 100–105. [Google Scholar] [CrossRef]
  13. Yonekura, S.; Okamoto, Y.; Yamasaki, K.; Horiguchi, S.; Hanazawa, T.; Matsune, S.; Kurono, Y.; Yamada, T.; Fujieda, S.; Okano, M.; et al. A randomized, double-blind, placebo-controlled study of ten-cha (rubus suavissimus) on house dust mite allergic rhinitis. Auris Nasus Larynx 2011, 38, 600–607. [Google Scholar] [CrossRef]
  14. Matkovic, Z.; Zivkovic, V.; Korica, M.; Plavec, D.; Pecanic, S.; Tudoric, N. Efficacy and safety of astragalus membranaceus in the treatment of patients with seasonal allergic rhinitis. Phytother. Res. 2010, 24, 175–181. [Google Scholar] [CrossRef]
  15. Swamy, S.M.; Tan, B.K. Cytotoxic and immunopotentiating effects of ethanolic extract of nigella sativa l. Seeds. J. Ethnopharmacol. 2000, 70, 1–7. [Google Scholar] [CrossRef]
  16. Isik, H.; Cevikbas, A.; Gurer, U.S.; Kiran, B.; Uresin, Y.; Rayaman, P.; Rayaman, E.; Gurbuz, B.; Buyukozturk, S. Potential adjuvant effects of nigella sativa seeds to improve specific immunotherapy in allergic rhinitis patients. Med. Princ. Pract. 2010, 19, 206–211. [Google Scholar] [CrossRef]
  17. Nikakhlagh, S.; Rahim, F.; Aryani, F.H.; Syahpoush, A.; Brougerdnya, M.G.; Saki, N. Herbal treatment of allergic rhinitis: The use of nigella sativa. Am. J. Otolaryngol. 2011, 32, 402–407. [Google Scholar] [CrossRef]
  18. Blom, H.M.; Godthelp, T.; Fokkens, W.J.; Klein Jan, A.; Holm, A.F.; Vroom, T.M.; Rijntjes, E. Mast cells, eosinophils and ige-positive cells in the nasal mucosa of patients with vasomotor rhinitis. An immunohistochemical study. Eur. Arch. Otorhinolaryngol. 1995, 252, S33–S39. [Google Scholar] [CrossRef]
  19. Philip, G.; Togias, A.G. Nonallergic rhinitis. Pathophysiology and models for study. Eur. Arch. Otorhinolaryngol. 1995, 252, S27–S32. [Google Scholar] [CrossRef]
  20. Wolf, G.; Anderhuber, W.; Hauser-Kronberger, C.; Saria, A. Treatment of nonspecific hyper-reflectory rhinopathy (vasomotor rhinitis) with capsaicin. Laryngorhinootologie 1995, 74, 289–293. [Google Scholar] [CrossRef]
  21. Ciabatti, P.G.; D’Ascanio, L. Intranasal capsicum spray in idiopathic rhinitis: A randomized prospective application regimen trial. Acta Otolaryngol. 2009, 129, 367–371. [Google Scholar] [CrossRef]
  22. Timmer, A.; Gunther, J.; Rucker, G.; Motschall, E.; Antes, G.; Kern, W.V. Pelargonium sidoides extract for acute respiratory tract infections. Cochrane Database Syst. Rev. 2008. [Google Scholar]
  23. Lizogub, V.G.; Riley, D.S.; Heger, M. Efficacy of a pelargonium sidoides preparation in patients with the common cold: A randomized, double blind, placebo-controlled clinical trial. Explore 2007, 3, 573–584. [Google Scholar] [CrossRef]
  24. Bachert, C.; Schapowal, A.; Funk, P.; Kieser, M. Treatment of acute rhinosinusitis with the preparation from pelargonium sidoides eps 7630: A randomized, double-blind, placebo-controlled trial. Rhinology 2009, 47, 51–58. [Google Scholar]
  25. Kolodziej, H.; Kiderlen, A.F. In vitro evaluation of antibacterial and immunomodulatory activities of pelargonium reniforme, pelargonium sidoides and the related herbal drug preparation eps 7630. Phytomedicine 2007, 14, 18–26. [Google Scholar] [CrossRef]
  26. Pelargonium (umckaloabo) hepatotoxisch? Arznei-telegramm 2006, 37, 41–42.
  27. Kehrl, W.; Sonnemann, U.; Dethlefsen, U. Therapy for acute nonpurulent rhinosinusitis with cineole: Results of a double-blind, randomized, placebo-controlled trial. Laryngoscope 2004, 114, 738–742. [Google Scholar] [CrossRef]
  28. Tesche, S.; Metternich, F.; Sonnemann, U.; Engelke, J.C.; Dethlefsen, U. The value of herbal medicines in the treatment of acute non-purulent rhinosinusitis. Results of a double-blind, randomised, controlled trial. Eur. Arch. Otorhinolaryngol. 2008, 265, 1355–1359. [Google Scholar] [CrossRef]
  29. Seo, B.S.; Lee, H.J.; Mo, J.H.; Lee, C.H.; Rhee, C.S.; Kim, J.W. Treatment of postviral olfactory loss with glucocorticoids, ginkgo biloba, and mometasone nasal spray. Arch. Otolaryngol. Head Neck Surg. 2009, 135, 1000–1004. [Google Scholar] [CrossRef]
  30. Boskabady, M.H.; Javan, H.; Sajady, M.; Rakhshandeh, H. The possible prophylactic effect of nigella sativa seed extract in asthmatic patients. Fundam. Clin. Pharmacol. 2007, 21, 559–566. [Google Scholar] [CrossRef]
  31. Belcaro, G.; Luzzi, R.; Cesinaro Di Rocco, P.; Cesarone, M.R.; Dugall, M.; Feragalli, B.; Errichi, B.M.; Ippolito, E.; Grossi, M.G.; Hosoi, M.; et al. Pycnogenol(r) improvements in asthma management. Panminerva Med. 2011, 53, 57–64. [Google Scholar]
  32. Hoang, B.X.; Shaw, D.G.; Levine, S.; Hoang, C.; Pham, P. New approach in asthma treatment using excitatory modulator. Phytother. Res. 2007, 21, 554–557. [Google Scholar] [CrossRef]
  33. Hong, M.H.; Lee, J.Y.; Jung, H.; Jin, D.H.; Go, H.Y.; Kim, J.H.; Jang, B.H.; Shin, Y.C.; Ko, S.G. Sophora flavescens aiton inhibits the production of pro-inflammatory cytokines through inhibition of the nf kappab/ikappab signal pathway in human mast cell line (hmc-1). Toxicol. In Vitro 2009, 23, 251–258. [Google Scholar] [CrossRef]
  34. Watson, R.R.; Zibadi, S.; Rafatpanah, H.; Jabbari, F.; Ghasemi, R.; Ghafari, J.; Afrasiabi, H.; Foo, L.Y.; Faridhosseini, R. Oral administration of the purple passion fruit peel extract reduces wheeze and cough and improves shortness of breath in adults with asthma. Nutr. Res. 2008, 28, 166–171. [Google Scholar] [CrossRef]
  35. Thomas, M.; Sheran, J.; Smith, N.; Fonseca, S.; Lee, A.J. Akl1, a botanical mixture for the treatment of asthma: A randomised, double-blind, placebo-controlled, cross-over study. BMC Pulm. Med. 2007, 7, 4. [Google Scholar] [CrossRef]
  36. Wong, E.L.; Sung, R.Y.; Leung, T.F.; Wong, Y.O.; Li, A.M.; Cheung, K.L.; Wong, C.K.; Fok, T.F.; Leung, P.C. Randomized, double-blind, placebo-controlled trial of herbal therapy for children with asthma. J. Altern. Complement. Med. 2009, 15, 1091–1097. [Google Scholar] [CrossRef]
  37. Jacobs, B.; Young, N.L.; Dick, P.T.; Ipp, M.M.; Dutkowski, R.; Davies, H.; Langley, J.M.; Greenberg, S.; Stephens, D.; Wang, E.E.L. Canadian acute respiratory illness and flu scale (carifs): Development of a valid measure for childhood respiratory infections. J. Clin. Epidemiol. 2000, 53, 793–799. [Google Scholar] [CrossRef]
  38. Kayser, O.; Kolodziej, H.; Kiderlen, A.F. Immunomodulatory principles of pelargonium sidoides. Phytother. Res. 2001, 15, 122–126. [Google Scholar] [CrossRef]
  39. Matthys, H.; Kamin, W.; Funk, P.; Heger, M. Pelargonium sidoides preparation (eps 7630) in the treatment of acute bronchitis in adults and children. Phytomedicine 2007, 14, 69–73. [Google Scholar] [CrossRef]
  40. Schulz, V. Liquid herbal drug preparation from the root of pelargonium sidoides is effective against acute bronchitis: Results of a double-blind study with 124 patients. Phytomedicine 2007, 14, 74–75. [Google Scholar] [CrossRef]
  41. Matthys, H.; Lizogub, V.G.; Malek, F.A.; Kieser, M. Efficacy and tolerability of eps 7630 tablets in patients with acute bronchitis: A randomised, double-blind, placebo-controlled dose-finding study with a herbal drug preparation from pelargonium sidoides. Curr. Med. Res. Opin. 2010, 26, 1413–1422. [Google Scholar] [CrossRef]
  42. Kemmerich, B. Evaluation of efficacy and tolerability of a fixed combination of dry extracts of thyme herb and primrose root in adults suffering from acute bronchitis with productive cough. A prospective, double-blind, placebo-controlled multicentre clinical trial. Arzneimittelforschung 2007, 57, 607–615. [Google Scholar]
  43. Fazio, S.; Pouso, J.; Dolinsky, D.; Fernandez, A.; Hernandez, M.; Clavier, G.; Hecker, M. Tolerance, safety and efficacy of hedera helix extract in inflammatory bronchial diseases under clinical practice conditions: A prospective, open, multicentre postmarketing study in 9657 patients. Phytomedicine 2009, 16, 17–24. [Google Scholar] [CrossRef]
  44. Cwientzek, U.; Ottillinger, B.; Arenberger, P. Acute bronchitis therapy with ivy leaves extracts in a two-arm study. A double-blind, randomised study vs. An other ivy leaves extract. Phytomedicine 2011, 18, 1105–1109. [Google Scholar] [CrossRef]
  45. Hudson, J.; Altamirano, M. The application of DNA micro-arrays (gene arrays) to the study of herbal medicines. J. Ethnopharmacol. 2006, 108, 2–15. [Google Scholar] [CrossRef]
  46. Gertsch, J.; Schoop, R.; Kuenzle, U.; Suter, A. Echinacea alkylamides modulate tnf-alpha gene expression via cannabinoid receptor cb2 and multiple signal transduction pathways. FEBS Lett. 2004, 577, 563–569. [Google Scholar] [CrossRef]
  47. Schapowal, A.; Berger, D.; Klein, P.; Suter, A. Echinacea/sage or chlorhexidine/lidocaine for treating acute sore throats: A randomized double-blind trial. Eur. J. Med. Res. 2009, 14, 406–412. [Google Scholar] [CrossRef]
  48. Goto, F.; Asama, Y.; Ogawa, K. Sho-saiko-to-ka-kikyo-sekko as an alternative treatment for chronic tonsillitis to avoid surgery. Complement. Ther. Clin. Pract. 2010, 16, 216–218. [Google Scholar] [CrossRef]
  49. Barrett, B.; Brown, R.; Rakel, D.; Mundt, M.; Bone, K.; Barlow, S.; Ewers, T. Echinacea for treating the common cold: A randomized trial. Ann. Int. Med. 2010, 153, 769–777. [Google Scholar]
  50. Roll, S.; Nocon, M.; Willich, S.N. Reduction of common cold symptoms by encapsulated juice powder concentrate of fruits and vegetables: A randomised, double-blind, placebo-controlled trial. Br. J. Nutr. 2011, 105, 118–122. [Google Scholar] [CrossRef]
  51. Rowe, C.A.; Nantz, M.P.; Bukowski, J.F.; Percival, S.S. Specific formulation of camellia sinensis prevents cold and flu symptoms and enhances gamma, delta t cell function: A randomized, double-blind, placebo-controlled study. J. Am. Coll. Nutr. 2007, 26, 445–452. [Google Scholar]
  52. Kubo, T.; Nishimura, H. Antipyretic effect of mao-to, a japanese herbal medicine, for treatment of type a influenza infection in children. Phytomedicine 2007, 14, 96–101. [Google Scholar] [CrossRef]
  53. Wang, L.; Zhang, R.M.; Liu, G.Y.; Wei, B.L.; Wang, Y.; Cai, H.Y.; Li, F.S.; Xu, Y.L.; Zheng, S.P.; Wang, G. Chinese herbs in treatment of influenza: A randomized, double-blind, placebo-controlled trial. Respir. Med. 2010, 104, 1362–1369. [Google Scholar] [CrossRef]
  54. Friedman, M. Overview of antibacterial, antitoxin, antiviral, and antifungal activities of tea flavonoids and teas. Mol. Nutr. food Res. 2007, 51, 116–134. [Google Scholar] [CrossRef]
  55. Kalus, U.; Kiesewetter, H.; Radtke, H. Effect of cystus052 and green tea on subjective symptoms in patients with infection of the upper respiratory tract. Phytother Res. 2010, 24, 96–100. [Google Scholar] [CrossRef]
  56. Wang, M.; Guilbert, L.J.; Li, J.; Wu, Y.; Pang, P.; Basu, T.K.; Shan, J.J. A proprietary extract from north american ginseng (panax quinquefolium) enhances il-2 and ifn-gamma productions in murine spleen cells induced by con-a. Int. Immunopharmacol. 2004, 4, 311–315. [Google Scholar] [CrossRef]
  57. Vohra, S.; Johnston, B.C.; Laycock, K.L.; Midodzi, W.K.; Dhunnoo, I.; Harris, E.; Baydala, L. Safety and tolerability of north american ginseng extract in the treatment of pediatric upper respiratory tract infection: A phase ii randomized, controlled trial of 2 dosing schedules. Pediatrics 2008, 122, e402–e410. [Google Scholar]
  58. Saxena, R.C.; Singh, R.; Kumar, P.; Yadav, S.C.; Negi, M.P.; Saxena, V.S.; Joshua, A.J.; Vijayabalaji, V.; Goudar, K.S.; Venkateshwarlu, K.; et al. A randomized double blind placebo controlled clinical evaluation of extract of andrographis paniculata (kalmcold) in patients with uncomplicated upper respiratory tract infection. Phytomedicine 2010, 17, 178–185. [Google Scholar] [CrossRef]
  59. Simpson, C.R.; Hippisley-Cox, J.; Sheikh, A. Trends in the epidemiology of chronic obstructive pulmonary disease in england: A national study of 51 804 patients. Br. J. Gen. Pract. 2010, 60, 277–284. [Google Scholar] [CrossRef]
  60. Shinozuka, N.; Tatsumi, K.; Nakamura, A.; Terada, J.; Kuriyama, T. The traditional herbal medicine hochuekkito improves systemic inflammation in patients with chronic obstructive pulmonary disease. J. Am. Geriatr. Soc. 2007, 55, 313–314. [Google Scholar] [CrossRef]
  61. Isbaniah, F.; Wiyono, W.H.; Yunus, F.; Setiawati, A.; Totzke, U.; Verbruggen, M.A. Echinacea purpurea along with zinc, selenium and vitamin c to alleviate exacerbations of chronic obstructive pulmonary disease: Results from a randomized controlled trial. J. Clin. Pharm. Ther. 2011, 36, 568–576. [Google Scholar] [CrossRef]
  62. Raduner, S.; Majewska, A.; Chen, J.Z.; Xie, X.Q.; Hamon, J.; Faller, B.; Altmann, K.H.; Gertsch, J. Alkylamides from echinacea are a new class of cannabinomimetics. Cannabinoid type 2 receptor-dependent and -independent immunomodulatory effects. J. Biol. Chem. 2006, 281, 14192–14206. [Google Scholar]
  63. Juergens, U.R.; Dethlefsen, U.; Steinkamp, G.; Gillissen, A.; Repges, R.; Vetter, H. Anti-inflammatory activity of 1.8-cineol (eucalyptol) in bronchial asthma: A double-blind placebo-controlled trial. Respir. Med. 2003, 97, 250–256. [Google Scholar] [CrossRef]
  64. Worth, H.; Schacher, C.; Dethlefsen, U. Concomitant therapy with cineole (eucalyptole) reduces exacerbations in copd: A placebo-controlled double-blind trial. Respir. Res. 2009, 10, 69. [Google Scholar] [CrossRef]
  65. Wahl, R.A.; Aldous, M.B.; Worden, K.A.; Grant, K.L. Echinacea purpurea and osteopathic manipulative treatment in children with recurrent otitis media: A randomized controlled trial. BMC Complement. Altern. Med. 2008, 8, 56. [Google Scholar] [CrossRef]
  66. Morgenstern, C.; Biermann, E. The efficacy of ginkgo special extract egb 761 in patients with tinnitus. Int. J. Clin. Pharmacol. Ther. 2002, 40, 188–197. [Google Scholar]
  67. Reisser, C.H.; Weidauer, H. Ginkgo biloba extract egb 761 or pentoxifylline for the treatment of sudden deafness: A randomized, reference-controlled, double-blind study. Acta Otolaryngol. 2001, 121, 579–584. [Google Scholar] [CrossRef]
  68. Burschka, M.A.; Hassan, H.A.; Reineke, T.; van Bebber, L.; Caird, D.M.; Mosges, R. Effect of treatment with ginkgo biloba extract egb 761 (oral) on unilateral idiopathic sudden hearing loss in a prospective randomized double-blind study of 106 outpatients. Eur. Arch. Otorhinolaryngol. 2001, 258, 213–219. [Google Scholar] [CrossRef]
  69. Siegers, C.P.; Syed Ali, S.; Tegtmeier, M. Aescin and troxerutin as a successful combination for the treatment of inner ear perfusion disturbances. Phytomedicine 2008, 15, 160–163. [Google Scholar] [CrossRef]
  70. Sirtori, C.R. Aescin: Pharmacology, pharmacokinetics and therapeutic profile. Pharmacol. Res. 2001, 44, 183–193. [Google Scholar] [CrossRef]
  71. Osawa, K.; Yasuda, H.; Morita, H.; Takeya, K.; Itokawa, H. Macrocarpals h, i, and j from the leaves of eucalyptus globulus. J. Nat. Prod. 1996, 59, 823–827. [Google Scholar] [CrossRef]
  72. Nagata, H.; Inagaki, Y.; Tanaka, M.; Ojima, M.; Kataoka, K.; Kuboniwa, M.; Nishida, N.; Shimizu, K.; Osawa, K.; Shizukuishi, S. Effect of eucalyptus extract chewing gum on periodontal health: A double-masked, randomized trial. J. Periodontol. 2008, 79, 1378–1385. [Google Scholar] [CrossRef]
  73. Nayak, S.S.; Kumar, B.R.; Ankola, A.V.; Hebbal, M. The efficacy of terminalia chebula rinse on streptococcus mutans count in saliva and its effect on salivary ph. Oral health Prev. Dent. 2010, 8, 55–58. [Google Scholar]
  74. Babaee, N.; Mansourian, A.; Momen-Heravi, F.; Moghadamnia, A.; Momen-Beitollahi, J. The efficacy of a paste containing myrtus communis (myrtle) in the management of recurrent aphthous stomatitis: A randomized controlled trial. Clin. Oral Investig. 2010, 14, 65–70. [Google Scholar] [CrossRef]
  75. Hoseinpour, H.; Peel, S.A.; Rakhshandeh, H.; Forouzanfar, A.; Taheri, M.; Rajabi, O.; Saljoghinejad, M.; Sohrabi, K. Evaluation of rosa damascena mouthwash in the treatment of recurrent aphthous stomatitis: A randomized, double-blinded, placebo-controlled clinical trial. Quintessence Int. 2011, 42, 483–491. [Google Scholar]
  76. Tian, J.H.; Liu, L.S.; Shi, Z.M.; Zhou, Z.Y.; Wang, L. A randomized controlled pilot trial of “feiji recipe” on quality of life of non-small cell lung cancer patients. Am. J. Chin. Med. 2010, 38, 15–25. [Google Scholar] [CrossRef]
  77. Kuriyama, S.; Shimazu, T.; Ohmori, K.; Kikuchi, N.; Nakaya, N.; Nishino, Y.; Tsubono, Y.; Tsuji, I. Green tea consumption and mortality due to cardiovascular disease, cancer, and all causes in japan: The ohsaki study. JAMA 2006, 296, 1255–1265. [Google Scholar]
  78. Tsao, A.S.; Liu, D.; Martin, J.; Tang, X.M.; Lee, J.J.; El-Naggar, A.K.; Wistuba, I.; Culotta, K.S.; Mao, L.; Gillenwater, A.; et al. Phase ii randomized, placebo-controlled trial of green tea extract in patients with high-risk oral premalignant lesions. Cancer Prev. Res. (Phila) 2009, 2, 931–941. [Google Scholar] [CrossRef]
  79. Fujiki, H.; Suganuma, M.; Okabe, S.; Sueoka, E.; Suga, K.; Imai, K.; Nakachi, K.; Kimura, S. Mechanistic findings of green tea as cancer preventive for humans. Proc. Soc. Exp. Biol. Med. 1999, 220, 225–228. [Google Scholar]
  80. Cao, Y.; Cao, R. Angiogenesis inhibited by drinking tea. Nature 1999, 398, 381. [Google Scholar] [CrossRef]
  81. Yu, H.M.; Liu, Y.F.; Cheng, Y.F.; Hu, L.K.; Hou, M. Effects of rhubarb extract on radiation induced lung toxicity via decreasing transforming growth factor-beta-1 and interleukin-6 in lung cancer patients treated with radiotherapy. Lung Cancer 2008, 59, 219–226. [Google Scholar] [CrossRef]
  82. Widrig, R.; Suter, A.; Saller, R.; Melzer, J. Choosing between nsaid and arnica for topical treatment of hand osteoarthritis in a randomised, double-blind study. Rheumatol. Int. 2007, 27, 585–591. [Google Scholar] [CrossRef]
  83. Robertson, A.; Suryanarayanan, R.; Banerjee, A. Homeopathic arnica montana for post-tonsillectomy analgesia: A randomised placebo control trial. Homeopathy 2007, 96, 17–21. [Google Scholar] [CrossRef]
  84. Xu, F.; Zeng, W.; Mao, X.; Fan, G.K. The efficacy of melilotus extract in the management of postoperative ecchymosis and edema after simultaneous rhinoplasty and blepharoplasty. Aesthetic Plast. Surg. 2008, 32, 599–603. [Google Scholar] [CrossRef]
  85. Hipps, Y.G.; Hacker, Y.E.; Hoffmann, D.L.; Brinckmann, J.A.; Socci, R.R.; Rogers, D. Self-reported quality of life in complementary and alternative medicine treatment of chronic rhinosinusitis among african americans: A preliminary, open-label pilot study. J. Altern. Complement. Med. 2009, 15, 67–77. [Google Scholar] [CrossRef]
  86. Kusche, J. Good clinical practice and phytotherapy. Methods Find. Exp. Clin. Pharmacol. 1993, 15, 241–247. [Google Scholar]
  87. Srisurapanon, S.; Rungroeng, K.; Apibal, S.; Cherdrugsi, P.; Siripol, R.; Vanich-Angkul, V.; Timvipark, C. The effect of standardized ginseng extract on peripheral blood leukocytes and lymphocyte subsets: A preliminary study in young health adults. J. Med. Assoc. Thai. 1997, 80, S81–S85. [Google Scholar]
  88. Ernst, E. Herbal medicines: Where is the evidence? BMJ 2000, 321, 395–396. [Google Scholar] [CrossRef]
  89. Gillis, C.N. Panax ginseng pharmacology: A nitric oxide link? Biochem. Pharmacol. 1997, 54, 1–8. [Google Scholar] [CrossRef]
  90. Konkimalla, V.B.; Efferth, T. Evidence-based chinese medicine for cancer therapy. J. Ethnopharmacol. 2008, 116, 207–210. [Google Scholar] [CrossRef]

Share and Cite

MDPI and ACS Style

Ghazi-Moghadam, K.; Inançlı, H.M.; Bazazy, N.; Plinkert, P.K.; Efferth, T.; Sertel, S. Phytomedicine in Otorhinolaryngology and Pulmonology: Clinical Trials with Herbal Remedies. Pharmaceuticals 2012, 5, 853-874.

AMA Style

Ghazi-Moghadam K, Inançlı HM, Bazazy N, Plinkert PK, Efferth T, Sertel S. Phytomedicine in Otorhinolaryngology and Pulmonology: Clinical Trials with Herbal Remedies. Pharmaceuticals. 2012; 5(8):853-874.

Chicago/Turabian Style

Ghazi-Moghadam, Koosha, Hasan Mete Inançlı, Nazanin Bazazy, Peter K. Plinkert, Thomas Efferth, and Serkan Sertel. 2012. "Phytomedicine in Otorhinolaryngology and Pulmonology: Clinical Trials with Herbal Remedies" Pharmaceuticals 5, no. 8: 853-874.

Article Metrics

Back to TopTop