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Acupuncture for sequelae of Bell's palsy: a randomized controlled trial protocol

机译:针灸治疗贝尔麻痹后遗症:一项随机对照试验方案

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摘要

Objective Incomplete recovery from facial palsy has a long-term impact on the quality of life, and medical options for the sequelae of Bell's palsy are limited. Invasive treatments and physiotherapy have been employed to relieve symptoms, but there is limited clinical evidence for their effectiveness. Acupuncture is widely used on Bell's palsy patients in East Asia, but there is insufficient evidence for its effectiveness on Bell's palsy sequelae. The objective is to evaluate the efficacy and safety of acupuncture in patients with sequelae of Bell's palsy. Method/Design This study consists of a randomized controlled trial with two parallel arms: an acupuncture group and a waitlist group. The acupuncture group will receive acupuncture treatment three times per week for a total of 24 sessions over 8 weeks. Participants in the waitlist group will not receive any acupuncture treatments during this 8 week period, but they will participate in the evaluations of symptoms at the start of the study, at 5 weeks and at 8 weeks after randomization, at which point the same treatment as the acupuncture group will be provided. The primary outcome will be analyzed by the change in the Facial Disability Index (FDI) from baseline to week eight. The secondary outcome measures will include FDI from baseline to week five, House-Brackmann Grade, lip mobility, and stiffness scales. Trial registration Current Controlled-Trials ISRCTN43104115 ; registration date: 06 July 2010; the date of the first patient's randomization: 04 August 2010
机译:目的从面部麻痹中恢复不完全会对生活质量产生长期影响,并且贝尔麻痹后遗症的医疗选择受到限制。侵入疗法和物理疗法已被用于缓解症状,但是其有效性的临床证据有限。针灸在东亚的贝尔氏麻痹患者中广泛使用,但尚无足够证据证明其对贝尔氏麻痹后遗症有效。目的是评估针灸治疗贝尔麻痹后遗症的有效性和安全性。方法/设计这项研究由一项随机对照试验组成,该试验有两个平行组:针灸组和候补组。针灸组每周接受3次针灸治疗,共8周,共24次。等待列表组的参与者在这8周内将不会接受任何针灸治疗,但是他们将在研究开始时,随机分组后5周和8周时参加症状评估,此时与将提供针灸组。主要结果将通过面部残疾指数(FDI)从基线到第八周的变化进行分析。次要结果指标将包括从基线到第五周的FDI,House-Brackmann等级,嘴唇活动度和僵硬度等级。试用注册电流对照试验ISRCTN43104115;注册日期:2010年7月6日;首例患者随机分组的日期:2010年8月4日

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