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电针治疗特应性湿疹瘙痒:一项多中心、随机、假针刺对照试验的研究方案

Electroacupuncture for relieving itching in atopic eczema: study protocol for a multicenter, randomized, sham-controlled trial.

作者信息

Wang Si-Han, Liang Rui-Long, Yang Han, Cai Xiao-Ce, Wang Jiao, Sun Xiao-Ying, Chen Jia-le, Wang Chun-Xiao, Jiang Wen-Cheng, 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, China.

Institute of Dermatology, Shanghai Academy of Traditional Chinese Medicine, Shanghai, China.

出版信息

Front Med (Lausanne). 2023 Dec 20;10:1320230. doi: 10.3389/fmed.2023.1320230. eCollection 2023.

Abstract

BACKGROUND

Atopic eczema (AE) is a common atopic inflammatory skin disease affecting 2.1-4.9% of the population in different countries. Pruritus, one of the most burdensome symptoms, is often underestimated for the problems it can cause, creating a vicious loop of itching, scratching, and lichenification. Therefore, further research into practical and safe treatments that relieve itchy symptoms and enhance skin protection is key to overcoming AE. Acupuncture, with or without electrical stimulation, is one of the most commonly used therapeutic measures to treat AE. This trial aimed to objectively evaluate the efficacy and safety of the electroacupuncture (EA) antipruritic technique in AE pruritus and obtain high-level clinical evidence for the popularization and application of EA for AE.

METHODS AND ANALYSIS

This multicenter, single-blinded, randomized controlled trial is planned to transpire from April 15, 2023, to June 30, 2025. We will recruit 132 participants with AE (44 per group). Participants will be assigned randomly to three equal-sized groups: EA, sham electroacupuncture, and sham acupuncture. Treatment will be administered three times a week during the 2-week intervention phase. The primary outcome measure is the Visual Analog Scale, with a numeric rating scale to evaluate pruritus. Secondary outcome measures include the Eczema Area and Severity Index and Dermatology Life Quality Index. Other outcome measures include physical examination, serum IgE, and safety evaluation. The number, nature, and severity of adverse events will be carefully recorded.

TRIAL REGISTRATION

ClinicalTrials.gov, 22Y11922200. Registered 3 September 2022, https://register.clinicaltrials.gov.

摘要

背景

特应性皮炎(AE)是一种常见的特应性炎症性皮肤病,在不同国家影响着2.1%-4.9%的人口。瘙痒是最令人困扰的症状之一,因其可能引发的问题常被低估,从而形成瘙痒、搔抓和苔藓化的恶性循环。因此,进一步研究切实可行且安全的治疗方法以缓解瘙痒症状并增强皮肤保护,是攻克AE的关键。针刺疗法,无论有无电刺激,都是治疗AE最常用的治疗措施之一。本试验旨在客观评估电针(EA)止痒技术对AE瘙痒的疗效和安全性,并为EA在AE中的推广应用获取高级别临床证据。

方法与分析

本多中心、单盲、随机对照试验计划于2023年4月15日至2025年6月30日进行。我们将招募132名AE患者(每组44名)。参与者将被随机分为三个同等规模的组:EA组、假电针组和假针刺组。在为期2周的干预阶段,每周进行三次治疗。主要结局指标是视觉模拟量表,用数字评定量表评估瘙痒程度。次要结局指标包括湿疹面积和严重程度指数以及皮肤病生活质量指数。其他结局指标包括体格检查、血清IgE和安全性评估。将仔细记录不良事件的数量、性质和严重程度。

试验注册

ClinicalTrials.gov,22Y11922200。于2022年9月3日注册,https://register.clinicaltrials.gov

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f53f/10761491/0f2fcfebf9d2/fmed-10-1320230-g001.jpg

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