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Is low-dose amitriptyline effective in the management of chronic low back pain? Study protocol for a randomised controlled trial

机译:小剂量阿米替林对慢性下腰痛的治疗有效吗?随机对照试验的研究方案

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Background Low back pain is a major clinical and public health problem, with limited evidence-based treatments. Low-dose antidepressants are commonly used to treat pain in chronic low back pain. However, their efficacy is unproven. The aim of this pragmatic, double-blind, randomised, placebo-controlled trial is to determine whether low-dose amitriptyline (an antidepressant) is more effective than placebo in reducing pain in individuals with chronic low back pain. Methods/design One hundred and fifty individuals with chronic low back pain will be recruited through hospital and private medical and allied health clinics, advertising in local media and posting of flyers in community locations. They will be randomly allocated to receive either low-dose amitriptyline (25?mg) or an active placebo (benztropine mesylate, 1?mg) for 6?months. The primary outcome measure of pain intensity will be assessed at baseline, 3 and 6?months using validated questionnaires. Secondary measures of self-reported low back disability, work absence and hindrance in the performance of paid/unpaid work will also be examined. Intention-to-treat analyses will be performed. Discussion This pragmatic, double-blind, randomised, placebo-controlled trial will provide evidence regarding the effectiveness of low-dose antidepressants compared with placebo in reducing pain, disability, work absenteeism and hindrance in work performance in individuals with chronic low back pain. This trial has major public health and clinical importance as it has the potential to provide an effective approach to the management of chronic low back pain. Trial registration Australian New Zealand Clinical Trials Registry: ACTRN12612000131853 ; registered on 30 January 2012.
机译:背景技术腰痛是临床和公共卫生的主要问题,采用循证医学的治疗方法有限。低剂量抗抑郁药通常用于治疗慢性下腰痛。但是,它们的功效尚未得到证实。这项务实,双盲,随机,安慰剂对照试验的目的是确定低剂量阿米替林(抗抑郁药)是否比安慰剂在减轻慢性腰背痛患者的疼痛方面更有效。方法/设计将通过医院和私人医疗诊所及专职医疗诊所招募150名慢性腰背痛患者,在当地媒体上刊登广告,并在社区内张贴传单。他们将被随机分配接受小剂量阿米替林(25?mg)或活性安慰剂(甲磺酸苯卓平,1?mg)治疗6个月。疼痛强度的主要结局指标将在基线,3和6个月时使用经过验证的问卷进行评估。自我报告的腰背残疾,缺勤和有偿/无偿工作表现受阻的次要措施也将进行检查。将进行意向治疗分析。讨论该实用,双盲,随机,安慰剂对照试验将提供证据,证明与安慰剂相比,低剂量抗抑郁药在减轻慢性腰背痛患者的疼痛,残疾,缺勤和工作表现方面的有效性。该试验具有重要的公共卫生和临床意义,因为它有可能为慢性下腰痛的治疗提供有效的方法。试验注册澳大利亚新西兰临床试验注册中心:ACTRN12612000131853; 2012年1月30日注册。

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