Suppr超能文献

腕管综合征腕夹板治疗的随机安慰剂对照试验研究方案。

Treatment of carpal tunnel syndrome with wrist splinting: study protocol for a randomized placebo-controlled trial.

机构信息

Department of Clinical Sciences - Orthopedics, Lund University, SE-22100, Lund, Sweden.

Department of Orthopedics Hässleholm-Kristianstad, Hässleholm Hospital, SE-28125, Hässleholm, Sweden.

出版信息

Trials. 2019 Aug 27;20(1):531. doi: 10.1186/s13063-019-3635-6.

Abstract

BACKGROUND

Carpal tunnel syndrome (CTS) is a common cause of pain, weakness, sensory loss, and activity limitations. Currently, the most common initial treatment is use of a rigid splint immobilizing the wrist, usually during night-time, for several weeks. Evidence regarding the efficacy and effect durability of wrist splinting is weak. The treatment is associated with costs and may cause discomfort and limit daily and work activities. No placebo-controlled trials have been performed.

METHODS

This is a randomized controlled trial designed to assess the efficacy of a rigid wrist splint compared with soft wrist bandage (placebo) in patients with primary idiopathic CTS. The trial will be conducted at an orthopedic department. Patients, 25 to 65 years old, who seek primary health-care with symptoms of CTS will be screened, and potentially eligible patients will be referred to the study center. Patients who fulfill the trial's eligibility criteria will be invited to participate. A total of 112 patients who provide informed consent will be randomly assigned to treatment with either a rigid wrist splint or a soft bandage to be used initially for 6 weeks at night and, if possible, during the day. The splints and bandages will be fitted with a temperature-monitoring device to measure the total time during which they have actually been worn. The trial participants will complete a questionnaire that includes the 6-item CTS symptoms scale (CTS-6); the 11-item disabilities of the arm, shoulder, and hand (QuickDASH) scale; and the EuroQol 5-dimension (EQ-5D) health status and quality-of-life measure at baseline and at 6, 12, 24, and 52 weeks after treatment start. The participants will undergo physical examination and nerve conduction testing at baseline and at 52 weeks. The trial's primary outcomes are the change in the CTS-6 score from baseline to 12 weeks and the rate of carpal tunnel release surgery at 52 weeks.

DISCUSSION

This is the first placebo-controlled randomized trial with electronic monitoring of actual splint use and will provide evidence regarding the efficacy of wrist splinting in patients with CTS.

TRIAL REGISTRATION

ISRCTN Registry, ISRCTN81836603 . Registered on May 5, 2018.

摘要

背景

腕管综合征(CTS)是引起疼痛、无力、感觉丧失和活动受限的常见原因。目前,最常见的初始治疗是使用刚性夹板固定手腕,通常在夜间持续数周。关于手腕夹板治疗的疗效和效果持久性的证据很薄弱。这种治疗方法会产生费用,并可能引起不适,限制日常和工作活动。目前还没有进行安慰剂对照试验。

方法

这是一项随机对照试验,旨在评估与软腕带(安慰剂)相比,原发性特发性 CTS 患者使用刚性腕夹板的疗效。该试验将在骨科部门进行。年龄在 25 至 65 岁之间,因 CTS 症状寻求初级保健的患者将进行筛查,有资格的潜在患者将被转诊到研究中心。符合试验入选标准的患者将被邀请参加。共有 112 名签署知情同意书的患者将被随机分配到刚性腕夹板或软绷带治疗组,两组患者均在夜间(如果可能的话,白天也使用)初始使用 6 周。夹板和绷带将配备温度监测装置,以测量实际佩戴的总时间。试验参与者将在基线和治疗开始后 6、12、24 和 52 周时完成包括 6 项 CTS 症状量表(CTS-6)、11 项手臂、肩部和手部残疾量表(QuickDASH)和欧洲五维健康量表(EQ-5D)健康状况和生活质量量表在内的问卷。参与者将在基线和 52 周时进行体格检查和神经传导测试。试验的主要结局是从基线到 12 周 CTS-6 评分的变化和 52 周时腕管松解手术的发生率。

讨论

这是第一项使用电子监测实际夹板使用情况的安慰剂对照随机试验,将为 CTS 患者使用手腕夹板的疗效提供证据。

试验注册

ISRCTN 注册处,ISRCTN81836603。于 2018 年 5 月 5 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3668/6712840/6ca41b93a0c0/13063_2019_3635_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验