Suppr超能文献

Jueyin颗粒治疗寻常型轻中度银屑病患者的疗效与安全性:一项多中心随机安慰剂对照试验方案

Efficacy and Safety of Jueyin Granules for Patients with Mild-to-Moderate Psoriasis Vulgaris: Protocol for a Multicenter Randomized Placebo-Controlled Trial.

作者信息

Li Su, Zhang Cang, Zhang Hong-Ya, Zhou Meng, Wang Si-Nong, Xu Rong, Zhou Dong-Mei, Ji Yun-Run, Lv Jing-Jing, Yin Qing-Feng, Wang Rui-Ping, Li Wei, Liu Yan-Ping, Wang Jian-Feng, Li Bin, Li Xin

机构信息

Department of Dermatology, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai 200437, China.

Department of Dermatology, Beijing Hospital of Traditional Chinese Medicine Affiliated to Capital Medical University, Beijing 100010, China.

出版信息

Evid Based Complement Alternat Med. 2020 Apr 9;2020:8942301. doi: 10.1155/2020/8942301. eCollection 2020.

Abstract

. The etiology and pathogenesis of psoriasis are complex. Blood-heat syndrome is the core pathogenesis of psoriasis. Based on theories of Chinese medicine (CM), heat-clearing and blood-cooling (HCBC) are the primary treatment. Very few studies have investigated the pharmacological mechanism of the CM HCBC method for treating psoriasis. This multicenter randomized controlled trial will focus on treating psoriasis blood-heat syndrome with the HCBC method using Jueyin granules (JYKL). This will be an objective and standardized evaluation of the efficacy, safety, and reproducibility of the HCBC method to obtain objective evidence meeting international standards that aim to establish a clinical standard suitable for the popular application of CM for treating psoriasis. . A five-center randomized double-blind placebo-controlled clinical design will be used in this study. At least 196 participants will be randomly assigned to receive either JYKL or placebo treatment approximately 30 minutes after meals in the morning and evening (one sachet per time, twice daily for 8 consecutive weeks). The study duration will be 17 weeks, including 1 week of screening, 8 weeks of intervention, and 8 weeks of follow-up. The patients will be evaluated every 2 weeks, and the measures will be compared with baseline values. The primary outcome measure will be the psoriasis lesion area severity index. We will also observe the recurrence rate, body surface area, physician global assessment, dermatology life quality index, quality of life index, visual analogue scale score, CM symptom score, combined drug use, and adverse events. This trial is registered with NCT03961230.

摘要

银屑病的病因和发病机制较为复杂。血热证是银屑病的核心发病机制。基于中医理论,清热凉血是主要治法。很少有研究探讨中医清热凉血法治疗银屑病的药理机制。这项多中心随机对照试验将聚焦于用厥阴颗粒(JYKL)以清热凉血法治疗银屑病血热证。这将对清热凉血法的疗效、安全性和可重复性进行客观、标准化评估,以获得符合国际标准的客观证据,旨在建立适合中医广泛应用于治疗银屑病的临床标准。 本研究将采用五中心随机双盲安慰剂对照的临床设计。至少196名参与者将被随机分配,在早晚饭后约30分钟接受JYKL或安慰剂治疗(每次1袋,每日2次,连续8周)。研究持续时间为17周,包括1周的筛查、8周的干预和8周的随访。患者每2周进行一次评估,并将测量结果与基线值进行比较。主要结局指标将是银屑病皮损面积严重程度指数。我们还将观察复发率、体表面积、医生整体评估、皮肤病生活质量指数、生活质量指数、视觉模拟量表评分、中医症状评分、联合用药情况及不良事件。本试验已在NCT03961230注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2a/7171628/ace2c732d812/ECAM2020-8942301.001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验