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加味逍遥汤治疗特应性皮炎合并胃肠功能紊乱患者的疗效与安全性:一项双盲、随机、安慰剂对照临床试验的研究方案

Efficacy and safety of Soshiho-tang in patients with atopic dermatitis and gastrointestinal disorders: Study protocol for a double-blind, randomized, and placebo-controlled clinical trial.

作者信息

Kang Su-Jin, Jo Eun-Heui, Yang Geum-Jin, Shim Yu-Hwa, Hong Ji-Eun, Park Min-Cheol

机构信息

Department of Korean Medicine Obstetrics & Gynecology, Won-Kwang University Korean Medicine Hospital, Iksan-si.

Department of Acupuncture and Moxibustion, Won-Kwang University Korean Medicine Hospital, Deokjin-gu, Jeonju-si.

出版信息

Medicine (Baltimore). 2019 May;98(18):e15479. doi: 10.1097/MD.0000000000015479.

Abstract

BACKGROUND

Atopic dermatitis (AD) is a chronically relapsing inflammatory skin disease that affects the quality of life in patients with AD. Since there is limitation of conventional treatment of AD, complementary treatment is required to treat AD symptoms more effectively and safely Soshiho-tang (SSHT) is a traditional herbal medicine that exhibits anti-inflammatory and anti-ulcer effects and improves the immune function. In this clinical trial, we will evaluate the efficacy and safety of SSHT in patients with AD and gastrointestinal disorders in comparison with placebo.

METHODS/DESIGN: This study is a single-center, randomized, double-blind, placebo-controlled, and investigator-initiated clinical trial. A total of 60 patients aged 3 to 18 years with AD and gastrointestinal disorders and who received a diagnosis of AD by Hanifin & Rajka criteria with a Scoring Atopic Dermatitis (SCORAD) index between 15 and 49 will be enrolled. Participants will be randomly assigned to the SSHT or placebo group in a ratio of 1:1. Additionally, they will have a visit schedule comprising 4 visits including a screening visit during 8 to 10 weeks. The participants will be administered SSHT or placebo 3 times a day for 4 weeks. The primary outcome will be measured by a change of the SCORAD index. The secondary outcome measures include the following: survey questionnaires for the perception of gastrointestinal disorders, amount and frequency of ointment usage for AD, dermatology quality of life index, itchiness and sleep disability score in visual analog scale, percutaneous water loss, skin surface temperature, Hamilton anxiety rating scale, and children's depression inventory.

DISCUSSION

In our knowledge, this will be the first clinical trial to assess the efficacy and safety of SSHT in patients with AD and gastrointestinal disorders. The findings of this study will provide new treatment options for patients with AD and gastrointestinal disorders.

TRIAL REGISTRATION

Korean National Clinical Trial Registry, Clinical Research Information Service. (KCT0003713) https://cris.nih.go.kr/cris/search/search_result_st01_en.jsp?seq=13489&ltype=&rtype=.

摘要

背景

特应性皮炎(AD)是一种慢性复发性炎症性皮肤病,会影响AD患者的生活质量。由于AD的传统治疗存在局限性,因此需要辅助治疗以更有效、安全地治疗AD症状。芍茜汤(SSHT)是一种传统草药,具有抗炎、抗溃疡作用,并能改善免疫功能。在这项临床试验中,我们将与安慰剂比较,评估SSHT对AD合并胃肠道疾病患者的疗效和安全性。

方法/设计:本研究是一项单中心、随机、双盲、安慰剂对照、研究者发起的临床试验。将招募60名年龄在3至18岁之间、患有AD和胃肠道疾病且根据Hanifin & Rajka标准被诊断为AD、特应性皮炎评分(SCORAD)指数在15至49之间的患者。参与者将按1:1的比例随机分配至SSHT组或安慰剂组。此外,他们将有一个包括4次就诊的访视计划,其中包括在8至10周内进行的筛查访视。参与者将接受SSHT或安慰剂治疗,每日3次,共4周。主要结局将通过SCORAD指数的变化来衡量。次要结局指标包括以下内容:胃肠道疾病认知调查问卷、AD外用软膏的使用量和频率、皮肤病生活质量指数、视觉模拟量表中的瘙痒和睡眠障碍评分、经皮水分流失、皮肤表面温度、汉密尔顿焦虑量表以及儿童抑郁量表。

讨论

据我们所知,这将是第一项评估SSHT对AD合并胃肠道疾病患者疗效和安全性的临床试验。本研究结果将为AD合并胃肠道疾病患者提供新的治疗选择。

试验注册

韩国国家临床试验注册中心,临床研究信息服务。(KCT0003713)https://cris.nih.go.kr/cris/search/search_result_st01_en.jsp?seq=13489&ltype=&rtype=

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ae2/6504306/6df2172b52d2/medi-98-e15479-g001.jpg

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