Efficacy of wearable transcutaneous electrical acupoint stimulation bracelet on moderate-to-severe postoperative nausea and vomiting in patients after general anesthesia: a study protocol for a multicenter randomized controlled trial.

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2024-12-02 DOI:10.1186/s13063-024-08650-4
Peng Ding, Dong-Yu Zheng, Hong-Wei Zhu, Ming Gong, Yong-Qiang Wang, Ling-Yan Jin, Guang-Li Ren, Hui-Jing Shi, Yong-Hua Li
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Abstract

Background: Postoperative nausea and vomiting (PONV) is the most common complication following general anesthesia. Currently, pharmaceutical therapy is the primary method of treatment, but it has reached a plateau, and it is accompanied by inherent adverse reactions and high costs. Stimulation of the wrist acupuncture point PC6 is recommended as an effective means of preventing PONV. Our previous study suggests that the wearable transcutaneous electrical acupoint stimulation (TEAS) bracelet can prevent PONV, but its effectiveness in treating moderate-to-severe PONV that has already occurred remains unknown. This trial aims to include female patients who have suffered from PONV after general anesthesia in real-world settings to investigate the therapeutic effect of the TEAS bracelet.

Methods: This trial will be conducted in Shanghai and Tianjin, China, with a total of 232 participants recruited from four academic hospitals. Participants will be randomly allocated into the TEAS group or the control group in a 1:1 ratio. Participants in the TEAS group will wear an EmeTerm bracelet and be injected with normal saline, while participants in the control group will wear a model bracelet and be injected with 10 mg of metoclopramide. Follow-up will be conducted 2 h later, and participants who do not experience relief will be randomly allocated into two groups and given cross-intervention. The primary outcome of the trial is the response rate of moderate-to-severe PONV after 2 h of intervention. Secondary outcomes include the recurrence rate of moderate-to-severe PONV within 24 h after intervention and the response rate of moderate-to-severe PONV at 2 h after cross-intervention in a population insensitive to the initial intervention.

Discussion: This multi-center randomized controlled trial aims to reveal the therapeutic effect of the wearable TEAS bracelet on PONV. It is expected that this bracelet will become an effective supplement for the clinical treatment of PONV, reducing medical expenditure and improving anesthesia quality and patient satisfaction.

Trial registration: Chinese Clinical Trial Registry ChiCTR2400084329. Registered on May 14, 2024.

可穿戴经皮穴位电刺激手环对全身麻醉患者术后中重度恶心呕吐的疗效:一项多中心随机对照试验研究方案
背景:术后恶心呕吐(PONV)是全麻后最常见的并发症。目前,药物治疗是主要的治疗方法,但它已经达到了一个平台期,并且伴随着固有的不良反应和高昂的费用。建议刺激手腕穴位PC6作为预防PONV的有效手段。我们之前的研究表明,可穿戴经皮穴位电刺激(TEAS)手环可以预防PONV,但其对已经发生的中重度PONV的治疗效果尚不清楚。该试验旨在纳入在现实环境中全身麻醉后患有PONV的女性患者,以研究TEAS手环的治疗效果。方法:本试验将在中国上海和天津进行,共从四家学术医院招募232名受试者。参与者将按1:1的比例随机分为tea组和对照组。tea组患者佩戴EmeTerm手环并注射生理盐水,对照组患者佩戴模型手环并注射10 mg甲氧氯普胺。2 h后进行随访,无缓解感的参与者随机分为两组,进行交叉干预。试验的主要结局是干预2小时后中重度PONV的缓解率。次要结局包括干预后24小时内中重度PONV的复发率和对初始干预不敏感人群交叉干预后2小时中重度PONV的缓解率。讨论:本多中心随机对照试验旨在揭示穿戴式TEAS手环对PONV的治疗效果。该手环有望成为PONV临床治疗的有效补充,降低医疗费用,提高麻醉质量和患者满意度。试验注册:中国临床试验注册中心ChiCTR2400084329。于2024年5月14日注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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