论文已发表
注册即可获取德孚的最新动态
IF 收录期刊
补肾祛寒止痛汤治疗类风湿关节炎临床深度缓解的疗效和安全性:一项双盲、随机、安慰剂对照试验方案
Authors Liu L , Wang J, Chen Y, Fang Y, Wang Z , Liu X, Hong L, Tao Q, Xu Y
Received 25 April 2025
Accepted for publication 12 August 2025
Published 21 August 2025 Volume 2025:18 Pages 4237—4249
DOI https://doi.org/10.2147/JPR.S536827
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 3
Editor who approved publication: Dr Alaa Abd-Elsayed
Longxiao Liu,1,2,* Jinping Wang,1,* Yanyu Chen,1,2 Yunlong Fang,1,2 Zihan Wang,1,2 Xiaojing Liu,1,2 Lidong Hong,1,2 Qingwen Tao,1 Yuan Xu1
1National Center for Integrative Medicine; Department of TCM Rheumatism, China-Japan Friendship Hospital, Beijing, People’s Republic of China; 2Graduate School, Beijing University of Chinese Medicine, Beijing, People’s Republic of China
*These authors contributed equally to this work
Correspondence: Qingwen Tao, Email taoqg1@sina.com Yuan Xu, Email xuyuan2004020@163.com
Purpose: Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by significant disability, with effective management of disease activity and pain constituting critical clinical objectives. The herbal formulation Bushen Quhan Zhiwang Decoction (BQZD) has demonstrated potential efficacy in symptom alleviation, suggesting a promising role in achieving sustained clinical remission in RA. The present study aims to systematically evaluate the efficacy and safety profile of BQZD for managing RA disease activity and pain relief.
Patients and Methods: This randomized, double-blind, placebo-controlled, single-center clinical trial will enroll a total of 72 RA patients, randomly assigning them into either the intervention group (n=36) receiving BQZD or the placebo control group (n=36). Participants will consume either BQZD or placebo (100 mL, twice daily) over a 12-week intervention period. Clinical assessments are scheduled at enrollment and subsequently at 4-week intervals, continuing through the 16-week mark post-intervention initiation. The primary outcome measure is the Disease Activity Score for 28 joints (DAS28). Secondary outcome variables include visual analogue scale (VAS) pain scores, mechanical pain threshold (MPT), central sensitization inventory (CSI), patient-reported outcomes (PROs), Traditional Chinese medicine (TCM) symptom scores, and biomarkers such as C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR). Safety endpoints will encompass monitoring of hematological parameters, urinalysis results, and adverse events.
Discussion: This study seeks to generate robust clinical evidence verifying the therapeutic efficacy and safety of BQZD for alleviating pain and achieving deep remission in RA patients. These findings are anticipated to facilitate broader integration of traditional herbal medicine within clinical practice. Additionally, this research endeavors to provide clinically relevant insights into precision treatments for RA by integrating traditional Chinese medicine and Western medical approaches, and aims to lay foundational evidence for future investigations into underlying regulatory mechanisms and potential therapeutic targets of TCM.
Keywords: rheumatoid arthritis, Bushen Quhan Zhiwang Decoction, clinical deep remission, pain, randomized controlled trial