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首页> 外文期刊>Trials >A randomised, multi-centre trial of total ankle replacement versus ankle arthrodesis in the treatment of patients with end stage ankle osteoarthritis (TARVA): statistical analysis plan
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A randomised, multi-centre trial of total ankle replacement versus ankle arthrodesis in the treatment of patients with end stage ankle osteoarthritis (TARVA): statistical analysis plan

机译:随机,多中心试验总踝部替代与踝关节关节术治疗末期踝关节骨关节炎(Tarva):统计分析计划

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摘要

The total ankle replacement versus ankle arthrodesis (TARVA) trial aims to determine which surgical procedure confers the greatest improvement in pain-free function for patients with end-stage ankle osteoarthritis. Both procedures are effective but there has not yet been a direct comparison to establish which is superior. This article describes the statistical analysis plan for this trial as an update to the published protocol. It is written prior to the end of patient follow-up, while the outcome of the trial is still unknown. TARVA is a randomised, un-blinded, parallel group trial of total ankle replacement versus ankle arthrodesis. The primary outcome is the Manchester-Oxford Foot Questionnaire walking/standing domain score at 52?weeks post-surgery. Secondary outcomes include measures of pain, social interaction, physical function, quality of life, and range of motion. We describe in detail the statistical aspects of TARVA: the outcome measures, the sample size calculation, general analysis principles including treatment of missing data, the planned descriptive statistics and statistical models, and planned subgroup and sensitivity analyses. The TARVA statistical analysis will provide comprehensive and precise information on the relative effectiveness of the two treatments. The plan will be implemented in January 2020 when follow-up for the trial is completed. ISRCTN registry number 60672307, ClinicalTrials.gov registration number NCT02128555. Registered 1 May 2014. Recruitment started in January 2015 and ended in January 2019.
机译:踝关节缩小剧本与踝关节关节术(Tarva)试验旨在确定哪种外科手术赋予最终阶段踝关节骨关节炎患者止痛功能的最大改善。这两个程序都有效,但尚未直接比较,建立优越。本文介绍了本试验的统计分析计划作为发布协议的更新。它是在患者随访结束之前写的,而试验的结果仍然是未知的。 Tarva是一个随机,未盲目的,平行的平行团体试验的总踝关节替代与踝关节痉挛。主要结果是曼彻斯特 - 牛津足部问卷行走/常规域名分数在52岁以下的手术后。二次结果包括痛苦,社会互动,物理功能,生活质量和运动范围的措施。我们详细描述了塔瓦的统计方面:结果措施,样本量计算,一般分析原则,包括缺失数据的治疗,计划的描述性统计模型以及计划的亚组和敏感性分析。 Tarva统计分析将提供有关两种治疗的相对效果的全面和精确的信息。该计划将于2012年1月在审判后续完成后实施。 ISRCTN注册表号60672307,ClinicalTrials.gov注册号NCT02128555。 2014年5月1日注册。招聘于2015年1月开始,并于2019年1月结束。

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