• J Ethnopharmacol · Jan 2013

    Randomized Controlled Trial Multicenter Study

    Efficacy and safety of Wuling capsule, a single herbal formula, in Chinese subjects with insomnia: a multicenter, randomized, double-blind, placebo-controlled trial.

    • Yan Lin, Xiao-yun Wang, Ren Ye, Wan-hua Hu, Shu-chen Sun, Hong-juan Jiao, Xiu-hua Song, Zheng-zhong Yuan, Yuan-yuan Zheng, Guo-qing Zheng, and Jin-Cai He.
    • The Second Affiliated Hospital of Wenzhou Medical College, Wenzhou 325027, China.
    • J Ethnopharmacol. 2013 Jan 9; 145 (1): 320-7.

    Ethnopharmacological RelevanceWuling Capsule is a single herbal formula from mycelia of precious Xylaria nigripes (Kl.) Sacc and its pharmacological function have a tranquilizing effect on the central nervous system. The aim of the study to evaluate the efficacy and safety of Wuling capsule in treatment of insomnia.Materials And MethodsWe performed a multicenter, randomized, double-blind, placebo-controlled study. The participants received either placebo (n=92) or Wuling capsule (n=94) for 4 weeks and a follow-up period for 2 weeks.ResultsCompared between pre-treatment and post-treatment, the global Pittsburgh sleep quality index (PSQI) scores in both Wuling capsule group and placebo group improved significantly (P<0.01). However, there was no significant difference between Wuling capsule group and placebo group (P>0.05). Scores of clinical global impressions scale (CGI-I) at each week in Wuling capsule group was similar to those in placebo group (P>0.05). Compared between pre-treatment and post-treatment, scores of the four components of world health organization on quality of life brief scale (WHOQOL-BREF) in both Wuling capsule group and placebo group improved significantly (P<0.01). However, there were no difference between the two groups (P>0.05). The rate of adverse events was 10.10% in Wuling group, and 6.73% in placebo group (P>0.05).ConclusionsWuling capsule can improve insomnia when compared with pre-treatment for 4 weeks and be a well tolerated by all the patients at the 6 weeks of study period. However, there are no significant in the results of the variables tested when compared with placebo control. Further additional rigorous randomized clinical trials are still required.Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.

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