Homeopathy for seasonal allergic rhinitis: rationale, design and methods of the three-armed randomized controlled HOMEOSAR trial

被引:0
|
作者
Siewert, J. [1 ,2 ,5 ]
Teut, M. [1 ,2 ,5 ]
Gaertner, K. [3 ]
Binting, S. [1 ,2 ,5 ]
Eberhardt, C. [4 ]
Ortiz, M. [1 ,2 ,5 ]
Grabowska, W. [1 ,2 ,5 ]
Reinhold, T. [1 ,2 ,5 ]
Roll, S. [1 ,2 ,5 ]
Stoeckigt, B. [1 ,2 ,5 ]
Willich, S. N. [1 ,2 ,5 ]
Cramer, H. [6 ]
Brinkhaus, B. [1 ,2 ,5 ]
机构
[1] Humboldt Univ, Inst Social Med Epidemiol & Hlth Econ, Berlin, Germany
[2] Free Univ Berlin, Berlin, Germany
[3] Univ Witten Herdecke, Inst Integrat Med, Herdecke, Germany
[4] Humboldt Univ, Pharm Dept, Berlin, Germany
[5] Humboldt Univ, Berlin, Germany
[6] Univ Duisburg Essen, Fac Med, Dept Internal & Integrat Med, Evang Kliniken Essen Mitte, Essen, Germany
关键词
Homeopathy; Complementary and alternative medicine; Allergy; Seasonal allergic rhinitis; Randomized controlled trial; QUALITY-OF-LIFE; ALTERNATIVE MEDICINE; DOUBLE-BLIND; NASAL SPRAY; PLACEBO; SAFETY; COMPLEMENTARY; ACUPUNCTURE; PREVALENCE; STATEMENT;
D O I
10.1186/s12906-022-03820-w
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background: Patients with seasonal allergic rhinitis (SAR) frequently use homeopathic therapy. Although there is some evidence that homeopathy may be effective in treating symptoms of SAR, there is a lack of high-quality clinical trials. Therefore, the aim of the homeopathy for SAR (HOMEOSAR) trial is to determine the efficacy of individualized or standardized homeopathic drug treatment compared to placebo regarding rhinitis-related quality of life in patients with SAR. Methods: This randomized, placebo-controlled, double-blind, three-armed intervention study will be conducted at two university hospital outpatient clinics for complementary and integrative medicine in Berlin and in 12 office-based practices specializing in homeopathic treatment in Germany. A total of 270 patients with clinical symptoms of SAR and positive allergy test to birch and grass pollen will receive homeopathic anamnesis and subsequently be randomized into (a) standardized homeopathic drug treatment with Galphimia Glauca (potency D6), (b) individualized homeopathic drug treatment (D6), or (c) placebo. All three groups can receive on-demand rescue medication as needed. Treatment will consist of two consultations and daily intake of the study medication for 4 weeks during the pollen season. The primary outcome is the mean overall score of the Rhinitis Quality of Life Questionnaire (RQLQ) in weeks 3 and 4, analyzed using analysis of covariance (adjusted for baseline RQLQ overall score and study center). A closed testing procedure will be used to control the overall type I error comparing the 3 treatment groups. Secondary outcomes include the overall RQLQ and its seven domain scores, responder status (decrease in RQLQ overall score of at least 0.5 points compared to the baseline value), use of rescue medication, intensity of total and individual SAR symptoms based on visual analog scale, generic health-related quality of life, safety, utilization of health care resources and associated costs. In addition, a qualitative data analysis is planned. Conclusion: The results of our study will contribute to clarifying the possible therapeutic effects of homeopathic drug treatment for patients with SAR.
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页数:9
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