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独活寄生汤治疗退行性膝骨关节炎的疗效、安全性及经济可行性:一项多中心、随机、评估者盲法、对照试验方案

Efficacy, Safety, and Economic Feasibility of Dokhwalgisaeng-Tang for Degenerative Knee Osteoarthritis: Protocol for a Multicenter, Randomized, Assessor Blinded, Controlled Trial.

作者信息

Kim Wonnam, Park Yeon-Cheol, Goo Bonhyuk, Kim Jung-Hyun, Nam Dongwoo, Kim Eunseok, Lee Hyun-Jong, Pyun Dong-Hyun, Suh Hae Sun, Lee Yoonsung, Kim Man S, Seo Byung-Kwan, Baek Yong-Hyeon

机构信息

Division of Pharmacology, School of Korean Medicine, Pusan National University, Yangsan, Republic of Korea.

Department of Acupuncture & Moxibustion, Kyung Hee University College of Korean Medicine, Kyung Hee University Hospital at Gangdong, Seoul, Republic of Korea.

出版信息

J Pain Res. 2024 Oct 28;17:3501-3510. doi: 10.2147/JPR.S487089. eCollection 2024.

Abstract

PURPOSE

Knee osteoarthritis (KOA) is one of the most prevalent degenerative joint diseases worldwide. The herbal decoction, Dokhwalgisaeng-tang (DHGST), has been commonly used in East Asia to treat osteoarthritis. However, there is insufficient evidence to draw clear conclusions concerning its effectiveness and safety for patients with KOA. We aim to determine the efficacy, safety, and economic feasibility of DHGST compared with Celecoxib, an oral COX-2 inhibitor, for patients with degenerative KOA.

TRIAL DESIGN AND METHODS

This multicenter, randomized, noninferiority trial, involving 160 participants who will be randomized using block randomization with 1:1 allocation, will compare DHGST and Celecoxib. The total trial period is 24 weeks after random allocation, comprising 12 weeks of treatment and 12 weeks of follow-up. Participants with KOA will be administered 200 mg of DHGST (treatment group) or Celecoxib capsules (control group) for 12 weeks. Efficacy and safety evaluations will be conducted at weeks 0, 4, 8, and 12, and 24. The primary outcome measurement is the Korean Western Ontario McMaster score at week 12. Changes in pain intensity using a 100 mm visual analog scale, changes in quality of life using a EuroQol 5-dimension 5-level self-report survey, and patient satisfaction will also be measured to evaluate effectiveness between the two groups. A trial-based economic feasibility evaluation will be conducted to analyze treatment cost-effectiveness from societal and healthcare system perspectives. Drug safety will be assessed through adverse reactions and laboratory test findings.

DISCUSSION

This trial protocol has the following limitations. Applying a double-dummy design is not possible, as the tablet and granule forms can easily be distinguished visually, and achieving participant blinding is challenging. The trial findings are intended to inform participants, physicians, and other stakeholders in determining whether DHGST could be used as an alternative therapeutic option for KOA.

TRIAL REGISTRATION NUMBER

KCT0008424 (Clinical Research Information Service of the Republic of Korea), registered on 12 May 2023.

摘要

目的

膝关节骨关节炎(KOA)是全球最常见的退行性关节疾病之一。草药汤剂独活寄生汤(DHGST)在东亚地区常用于治疗骨关节炎。然而,关于其对KOA患者的有效性和安全性,尚无足够证据得出明确结论。我们旨在确定与口服COX - 2抑制剂塞来昔布相比,DHGST对退行性KOA患者的疗效、安全性和经济可行性。

试验设计与方法

这项多中心、随机、非劣效性试验将纳入160名参与者,采用1:1分配的区组随机化方法进行随机分组,比较DHGST和塞来昔布。随机分配后的总试验期为24周,包括12周的治疗期和12周的随访期。KOA患者将接受200毫克DHGST(治疗组)或塞来昔布胶囊(对照组)治疗12周。在第0、4、8、12和24周进行疗效和安全性评估。主要结局指标是第12周时的韩国西部安大略和麦克马斯特大学骨关节炎指数(WOMAC)评分。还将使用100毫米视觉模拟量表测量疼痛强度变化,使用欧洲五维健康量表(EuroQol 5维度5水平)自我报告调查测量生活质量变化,并评估患者满意度,以评价两组之间的疗效。将从社会和医疗保健系统角度进行基于试验的经济可行性评估,分析治疗成本效益。通过不良反应和实验室检查结果评估药物安全性。

讨论

本试验方案有以下局限性。由于片剂和颗粒剂在视觉上易于区分,无法采用双盲设计,实现参与者盲法具有挑战性。试验结果旨在为参与者、医生和其他利益相关者提供信息,以确定DHGST是否可作为KOA的替代治疗选择。

试验注册号

KCT0008424(大韩民国临床研究信息服务中心),于2023年5月12日注册。

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