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Conservative management versus open reduction and internal fixation for mid-shaft clavicle fractures in adults - The Clavicle Trial: study protocol for a multicentre randomized controlled trial

机译:成年人保守治疗中轴锁骨骨折的保守治疗与切开复位内固定术-锁骨试验:一项多中心随机对照试验的研究方案

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Background Clavicle fractures account for around 4% of all fractures and up to 44% of fractures of the shoulder girdle. Fractures of the middle third (or mid-shaft) account for approximately 80% of all clavicle fractures. Management of this group of fractures is often challenging and the outcome can be unsatisfactory. In particular it is not clear whether surgery produces better outcomes than non-surgical management. Currently there is much variation in the use of surgery and a lack of good quality evidence to inform our decision. Methods/Design We aim to undertake a multicentre randomised controlled trial evaluating the effectiveness and safety of conservative management versus open reduction and internal fixation for displaced mid-shaft clavicle fractures in adults. Surgical treatment will be performed using the Acumed clavicle fixation system. Conservative management will consist of immobilisation in a sling at the side in internal rotation for 6 weeks or until clinical or radiological union. We aim to recruit 300 patients. These patients will be followed-up for at least 9 months. The primary endpoint will be the rate of non-union at 3 months following treatment. Secondary endpoints will be limb function measured using the Constant-Murley Score and the Disabilities of the Arm, Shoulder and Hand (DASH) Score at 3 and 9 months post-operatively. Discussion This article presents the protocol for a multicentre randomised controlled trial. It gives extensive details of, and the basis for, the chosen methods, and describes the key measures taken to avoid bias and to ensure validity. Trial Registration United Kingdom Clinical Research Network ID: 8665. The date of registration of the trial is 07/09/2006. The date the first patient was recruited is 18/12/2007.
机译:背景锁骨骨折约占所有骨折的4%,最多占肩带骨折的44%。中间三分之一(或中轴)骨折约占锁骨全部骨折的80%。这组骨折的治疗通常具有挑战性,结果可能不令人满意。特别是手术是否比非手术治疗效果更好尚不清楚。当前,外科手术的使用存在很大差异,并且缺乏高质量的证据来告知我们的决定。方法/设计我们的目标是进行一项多中心随机对照试验,评估成人移位中轴锁骨骨折保守治疗与切开复位内固定的有效性和安全性。手术治疗将使用Acumed锁骨固定系统进行。保守治疗将包括固定在一侧的悬带内旋转6周或直到临床或放射学结合为止。我们的目标是招募300名患者。这些患者将至少随访9个月。主要终点为治疗后3个月的骨不连率。次要终点是在术后3个月和9个月时使用Constant-Murley评分和手臂,肩膀和手部残疾(DASH)评分测量的肢体功能。讨论本文介绍了多中心随机对照试验的方案。它提供了所选方法的详细信息和基础,并介绍了为避免偏差和确保有效性而采取的关键措施。试验注册英国临床研究网络ID:8665。试验的注册日期为2006年9月9日。招募第一位患者的日期是18/12/2007。

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