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电针治疗结肠镜检查患者不适的效果:一项多中心、随机、对照临床试验方案

Effect of electroacupuncture on discomfort in patients undergoing colonoscopy: protocol for a multicentre, randomised, controlled clinical trial.

作者信息

Sun Xiangyu, Lu Liyue, Wang Yongqiang, Wang Chunchun, Lin Chao, Xu Kuangdi, Yong Yue, Chen Wenting, Song Jiangang

机构信息

Acupuncture Anesthesia Institute, Shanghai Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, Shanghai, China.

Department of Anesthesiology, Shanghai Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.

出版信息

BMJ Open. 2024 Dec 20;14(12):e084628. doi: 10.1136/bmjopen-2024-084628.

Abstract

INTRODUCTION

Colonoscopy is currently the most commonly used and effective method for early detection, diagnosis and treatment of tumours of the colon and rectum. However, similar to other invasive procedures, it is associated with adverse reactions such as pain and abdominal distension. Electroacupuncture (EA) has been proposed as a potential treatment for relieving this discomfort; however, there is limited evidence supporting its efficacy. Therefore, the aim of this study is to investigate the effectiveness of EA when used prior to colonoscopy.

METHODS AND ANALYSIS

This multicentre, randomised, controlled, patient-assessor-blinded trial will be conducted at three hospitals in China. A total of 500 participants will be randomly assigned to either the EA group or sham EA (SEA) group, in a 1:1 ratio. EA will be administered for 30 min before the colonoscopy. Participants will be asked to complete detailed questionnaires within 10 min after the procedure and 24 hours after the procedure to record their symptoms. The primary outcome will be assessed using discomfort numeric rating scale (NRS) scores. Secondary outcomes will include participants' tolerance levels, including standard NRS scores for abdominal pain, bloating and anal discomfort reported by the participants, as well as heart rate(HR), blood pressure(BP), surgical pleth index, participant satisfaction, nurses' and endoscopists' evaluations, incidence of adverse events and salivary cortisol levels collected before EA and after colonoscopy.

ETHICS AND DISSEMINATION

Ethics approval was obtained from the Ethics Committee of Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine (number 2023-1327-94-01), Ethics Committee of Longhua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine (number 2023LCSY059) and Ethics Committee of Wuxi Hospital Affiliated to Nanjing University of Traditional Chinese Medicine (number 2023-062-01). The results of this study will be disseminated in peer-reviewed publications. All potential participants will be provided informed consent before participating in the study.

TRIAL REGISTRATION NUMBER

ChiCTR2300073485.

摘要

引言

结肠镜检查是目前用于早期检测、诊断和治疗结肠及直肠肿瘤最常用且有效的方法。然而,与其他侵入性检查一样,它会引发疼痛和腹胀等不良反应。电针已被提议作为缓解这种不适的一种潜在治疗方法;然而,支持其疗效的证据有限。因此,本研究的目的是探讨结肠镜检查前使用电针的有效性。

方法与分析

本多中心、随机、对照、患者及评估者双盲试验将在中国的三家医院进行。总共500名参与者将按1:1的比例随机分配到电针组或假电针(SEA)组。结肠镜检查前将进行30分钟的电针治疗。参与者将被要求在检查后10分钟内和检查后24小时内完成详细问卷,以记录他们的症状。主要结局将使用不适数字评定量表(NRS)评分进行评估。次要结局将包括参与者的耐受水平,包括参与者报告的腹痛、腹胀和肛门不适的标准NRS评分,以及心率(HR)、血压(BP)、手术容积指数、参与者满意度、护士和内镜医师的评估、不良事件发生率以及电针治疗前和结肠镜检查后采集的唾液皮质醇水平。

伦理与传播

已获得上海中医药大学附属曙光医院伦理委员会(编号2023 - 1327 - 94 - 01)、上海中医药大学附属龙华医院伦理委员会(编号2023LCSY059)和南京中医药大学附属无锡医院伦理委员会(编号2023 - 062 - 01)的伦理批准。本研究结果将在同行评审的出版物上发表。所有潜在参与者在参与研究前将获得知情同意。

试验注册号

ChiCTR2300073485。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6a6/11667368/187fdabd9e01/bmjopen-14-12-g001.jpg

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