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The Chinese herbal formula Huoxiang Zhengqi for atopic dermatitis with dampness pattern (CHARM): a study protocol for a double-blinded randomized controlled trial

机译:中国草药配方鲍祥郑琪具有潮湿模式(魅力)的特应性皮炎:双盲随机对照试验的研究方案

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Background Atopic dermatitis (AD) is a complex, common inflammatory skin disease. The Chinese herbal formula Huoxiang Zhengqi (HXZQ) has been a common dermatosis treatment in China for many years, but there is no high-level evidence for its effect on AD/eczema. The aim of this trial is to examine the efficacy and safety of HXZQ treating AD/eczema patients. Methods This is a double-blind, multi-center, randomized controlled trial comparing HXZQ to a placebo. It will consist of 4?weeks’ treatment and 4?weeks of follow-up. A total of 218 participants will be randomly allocated into two groups—an HXZQ group and a placebo group, from 7 hospitals in China. Patients diagnosed with AD will be enrolled if they are in accordance with CM dampness pattern, have body surface area (BSA) of 1–10%, have investigator’s global assessment (IGA) of 1–3, have age between 18 and 70?years, and provide signed informed consent. The Eczema Area and Severity Index (EASI) is the primary outcome. The secondary outcomes are the numerical itch rating scale, IGA, BSA, Skindex-29, and EQ-5D-5L score, from baseline to the end of the treatment. Analysis will be on intention-to-treat and per-protocol subject analysis principles. Discussion The goal of this trial is to evaluate the efficacy and availability of HXZQ oral liquid in treating AD/eczema in terms of symptoms and eczematous lesions. It will also address whether it has positive effect on QoL. Trial registration Chinese Clinical Trial Registry ( http://www.chictr.org.cn/index.aspx ): Chinese herbal formula Huoxiang Zhengqi for atopic dermatitis with dampness pattern (CHARM): a double-blinded randomized controlled trial, ChiCTR1900026700 . Registered on 19 October 2019.
机译:背景特应患者皮炎(AD)是一种复杂的常见炎症皮肤病。中国草药配方Huoxiang Zhengqi(HXZQ)多年来一直是中国常见的皮肤病治疗,但没有高水平的证据证明其对广告/湿疹的影响。该试验的目的是检查HXZQ治疗AD /湿疹患者的疗效和安全性。方法这是一个双盲,多中心,随机对照试验,将HXZQ与安慰剂进行比较。它将包括4周的治疗和4个?几周的随访。共有218名参与者将随机分配为两组 - 一个HXZQ集团和一个安慰剂集团,来自中国的7家医院。患者患有AD的患者将注册,如果它们符合CM湿度模式,则具有1-10%的体表面积(BSA),具有1-3的调查员的全球评估(IGA),年龄在18至70岁之间,并提供签署的知情同意书。湿疹地区和严重程度指数(EASI)是主要结果。二次结果是数值瘙痒率,IGA,BSA,SkindEx-29和EQ-5D-5L分数,从基线到治疗结束。分析将在意向治疗和每协议主题分析原则上。讨论该试验的目标是评估HXZQ口服液在症状和湿疹病变方面治疗AD /湿疹的疗效和可用性。它还将解决它是否对QOL具有积极影响。试验登记中国临床试验登记处(http://www.chictr.org.cn/index.aspx):中草原逆风针对特应性皮炎的潮湿模式(魅力):一款双盲随机对照试验,CHICTR1900026700。注册于2019年10月19日。

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