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Journal of Integrative Medicine

   

Efficacy and safety of Huzhang Granule, a compound Chinse herbal medicine, for acute gouty arthritis: A double-blind, randomized controlled trial

Hao Wanga,b, Si-ting Chenc, Xiao-jie Dinga,b, Le Kuaia,b, Liang Huaa,b, Xin Lia,b, Yi-fei Wanga,b, Ming Zhanga,b, Bin Lib,d,e, Rui-ping Wangd, Mi Zhoua,b   

  1. a. Department of Dermatology, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai 200437, China
    b. Institute of Dermatology, Shanghai Academy of Traditional Chinese Medicine, Shanghai 201203, China
    c. Department of Dermatology, the Affiliated Hospital of Jiangxi University of Chinese Medicine, Nanchang 330000, Jiangxi Province, China
    d. Shanghai Skin Disease Hospital, School of Medicine, Tongji University, Shanghai 200443, China
    e. Institute of Dermatology, School of Medicine, Tongji University, Shanghai 200443, China
  • Received:2023-12-20 Accepted:2024-02-22 Online:2024-03-26 Published:2024-03-26
  • Contact: Mi Zhou; Rui-ping Wang E-mail:vieky2866@163.com; w19830901@126.com

Background

Acute gouty arthritis (AGA) is an inflammatory joint disease with a high prevalence. Typical medical interventions, including nonsteroidal anti-inflammatory drugs, colchicine and glucocorticoids, can have serious adverse reactions. Huzhang Granule (HZG), a compound Chinse herbal medicine, has been used to treat AGA for more than 30 years with satisfactory effects and no significant adverse reactions. However, the efficacy and safety of HZG in AGA patients remains unknown.

Objective

The present investigation was designed to examine the efficacy and safety profile of HZG in managing AGA patients.

Design, setting, participants and interventions

The current study was conducted as a noninferiority, randomized controlled clinical trial on 180 eligible enrolled participants. Participants were randomly assigned into the HZG and etoricoxib groups. Treatments were administered for 5 d, during which the HZG group received HZG and placebo etoricoxib, while the etoricoxib group received etoricoxib and placebo HZG in the same ratio (1:1).

Main outcome measures

The primary outcome was pain experienced by the patient in the gout-afflicted joint from days 2 to 5 of the treatment window. The pain level was measured via a visual analogue scale, ranging from 0 mm to 100 mm. The secondary outcomes comprised joint tenderness and swelling, reduction of inflammatory biomarkers, and the patient’s and investigator’s global evaluations of therapeutic response.

Results

The mean reduction in pain was –51.22 mm (95% confidence interval [CI], [–53.42, –49.03] mm) for the HZG and –52.00 mm (95% CI, [–54.06, –49.94] mm) for the etoricoxib groups. The mean difference between the two groups was 0.78 mm (95% CI, [–2.25, 3.81] mm). All additional efficacy endpoints, covering decreased inflammation and pain relief, yielded compelling proof of noninferiority. Patients in the HZG group exhibited a comparatively lower rate of adverse events compared to those in the etoricoxib group (4.44% vs 13.33%; P ≤ 0.05).

Conclusion

HZG and etoricoxib groups demonstrated similar levels of analgesic effectiveness. The safety and efficacy of HZG indicates that it can be used as a potential therapeutic option for treating AGA.

Trial registration

Chinese Clinical Trial Registry (ChiCTR2000036970).


Key words: Acute gouty arthritis, Huzhang Granule, Randomized controlled trial, Blind

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