Applied Research Collaboration South West Peninsula (PenARC), National Institute for Health and Care Research (NIHR), University of Exeter, Exeter, UK.
Exeter Clinical Trials Unit, University of Exeter Medical School, Exeter, UK.
Trials. 2022 Nov 5;23(1):924. doi: 10.1186/s13063-022-06790-z.
The HemiSPAIRE trial is being conducted to determine whether a modified muscle sparing technique (SPAIRE-"Save Piriformis and Internus, Repairing Externus") in hip hemiarthroplasty brings clinical benefits compared to the standard lateral technique in adults aged 60 years or older, with a displaced intracapsular hip fracture. This article describes the detailed statistical analysis plan for the trial. METHODS AND DESIGN: HemiSPAIRE is a definitive, pragmatic, superiority, multicentre, randomised controlled trial (with internal pilot) with two parallel groups. Participants, ward staff and all research staff involved in post-operative assessments are blinded to allocation. This article describes in detail (1) the primary and secondary outcomes; (2) the statistical analysis principles, including a survivor average causal effect (SACE) method chosen specifically to address the issue of potential bias from differential survival between trial arms, which was seen from data review by the Trial Steering Committee, the participants that will be included in each analysis, the covariates that will be included in each analysis, and how the results will be presented; (3) planned main analysis of the primary outcome; (4) planned analyses of the secondary outcomes; and (5) planned additional analyses of the primary and secondary outcomes.
ClinicalTrials.gov NCT04095611. Registered on 19 September 2019.
正在进行 HemiSPAIRE 试验,以确定在 60 岁或以上、有移位的囊内髋部骨折的成人中,与标准外侧技术相比,髋关节半髋关节置换术中改良的保留梨状肌和内旋肌、修复外旋肌技术(SPAIRE-“Save Piriformis and Internus, Repairing Externus”)是否具有临床益处。本文介绍了该试验的详细统计分析计划。
HemiSPAIRE 是一项明确的、实用的、优势的、多中心、随机对照试验(带内部预试验),有两个平行组。参与者、病房工作人员和参与术后评估的所有研究人员均对分组情况不知情。本文详细描述了(1)主要和次要结局;(2)统计分析原则,包括选择幸存者平均因果效应(SACE)方法专门解决试验组之间潜在生存差异的偏倚问题,这是试验指导委员会从数据审查中发现的,将纳入每个分析的参与者,将纳入每个分析的协变量,以及如何呈现结果;(3)主要结局的主要分析计划;(4)次要结局的分析计划;以及(5)主要和次要结局的额外分析计划。
ClinicalTrials.gov NCT04095611。于 2019 年 9 月 19 日注册。