Asia Pac Allergy.
2012 Jul;2(3):187-194. 10.5415/apallergy.2012.2.3.187.
Lack of efficacy of a herbal preparation (RCM-102) for seasonal allergic rhinitis: a double blind, randomised, placebo-controlled trial
- Affiliations
-
- 1Traditional & Complementary Medicine Research Program, Health Innovations Research Institute, Discipline of Chinese Medicine, School of Health Sciences, RMIT University, Bundoora Campus, Victoria 3083, Australia. george.lenon@rmit.edu.au
- 2Department of Respiratory Medicine, Box Hill Hospital & Monash University, Box Hill, Victoria 3128, Australia.
- KMID: 2397481
- DOI: http://doi.org/10.5415/apallergy.2012.2.3.187
Abstract
- BACKGROUND
A herbal preparation, known as RMIT Chinese Medicine 102 (RCM-102) consisting of eight herbs which demonstrates inhibition of the release of key inflammatory mediators associated with seasonal allergic rhinitis (SAR) was used. This study evaluated the efficacy and safety of RCM-102 for SAR.
OBJECTIVE
This study evaluated the efficacy and safety of RCM-102 for SAR.
METHODS
This randomised placebo-controlled trial involved subjects aged between 18 and 65 who were randomly assigned to either RCM-102 or a placebo group. After a two-week baseline period, all subjects took either RCM-102 or placebo capsules (two capsules each time, three times daily with a four hour interval) for a period of eight weeks. The primary end-points were the Five-Point Scale symptom scores. Rhinoconjunctivitis Quality of Life Questionnaire, relief medication usage, adverse events, kidney and liver function tests and full blood examination were secondary end-points. Intention-to-treat analysis was applied.
RESULTS
One hundred and four subjects were randomised with 52 in each group. Ninety-five subjects (47 and 48 subjects in RCM-102 and placebo groups) completed the trial. Nine subjects withdrew from the study prior to the end of the second treatment week. At the end of the trial, there were no significant differences between the two groups with respect to all outcome measures. There were no liver or kidney function abnormalities reported.
CONCLUSION
This mechanism-based RCM-102 was safe but not more beneficial than placebo for patients with SAR.
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