Oxford Clinical Trials Research Unit, Centre for Statistics in Medicine, Nuffield Department of Orthopaedics, Rheumatology, and Musculoskeletal Sciences, University of Oxford, Oxford, OX3 7LD, UK.
Surgical Interventional Trials Unit, Nuffield Department Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.
Trials. 2022 May 12;23(1):389. doi: 10.1186/s13063-022-06309-6.
Rupture of the anterior cruciate ligament (ACL) is a common injury, primarily affecting young, active individuals. Despite surgical intervention being the more common treatment for patients suffering ACL ruptures, current management is based on limited and generally low-quality evidence. We describe a statistical analysis plan (SAP) for the ACL SNNAP randomised controlled trial, which aims to investigate the necessity of surgical management in patients with ACL injuries.
METHODS/DESIGN: ACL SNNAP is a pragmatic, multi-centre, superiority, parallel-group randomised controlled trial in participants with a symptomatic non-acute ACL deficient knee. Participants are allocated in a 1:1 ratio to either non-surgical management (rehabilitation) or surgical management (reconstruction) with the aim of assessing the efficacy and cost-effectiveness. The primary outcome of the study is the Knee Injury and Osteoarthritis Outcome Score (KOOS4) at 18 months post-randomisation. The KOOS4 score at 18 months will be evaluated using a linear regression model adjusting for recruitment centre and baseline KOOS4 scores, allowing for intra-centre correlation. A secondary analysis of the primary outcome will be carried out using an area under the curve (AUC) approach using treatment estimates obtained from a mixed model using baseline, 6 months, 12 months, and 18 months post-randomisation outcome data. Secondary outcomes will be measured at 18 months and will include return to activity/level of sport participation, intervention-related complications, the EQ-5D-5L questionnaire, all 5 individual subscales of the KOOS questionnaire, the ACL-QOL score, expectations of return to activity and cost-effectiveness of the interventions. Missing primary outcome data will be investigated through a sensitivity analysis. Full details of the planned methods for the statistical analysis of clinical outcomes are presented in this paper. The study protocol for the ACL SNNAP trial has been published previously.
The methods of analysis for the ACL SNNAP trial have been described here to minimise the risk of data-driven results and reporting bias. Any deviations from the analysis methods described in this paper will be described in full and justified in the publications of the trial results.
ISRCTN ISRCTN10110685 . Registered on 16 November 2016.
前交叉韧带(ACL)断裂是一种常见的损伤,主要影响年轻、活跃的个体。尽管手术干预是 ACL 断裂患者更常见的治疗方法,但目前的治疗方法基于有限且通常质量较低的证据。我们描述了 ACL SNNAP 随机对照试验的统计分析计划(SAP),该试验旨在研究 ACL 损伤患者是否需要手术治疗。
方法/设计:ACL SNNAP 是一项在有症状的非急性 ACL 缺陷膝关节患者中进行的实用、多中心、优效性、平行组随机对照试验。参与者以 1:1 的比例分配到非手术治疗(康复)或手术治疗(重建),旨在评估疗效和成本效益。该研究的主要结局是随机分组后 18 个月的膝关节损伤和骨关节炎结果评分(KOOS4)。18 个月时的 KOOS4 评分将使用线性回归模型进行评估,该模型调整了招募中心和基线 KOOS4 评分,允许中心内相关性。主要结局的二次分析将使用基于曲线下面积(AUC)的方法进行,该方法使用从混合模型中获得的治疗估计值,该混合模型使用基线、6 个月、12 个月和随机分组后 18 个月的结局数据。次要结局将在 18 个月时测量,包括活动/运动参与水平的恢复、与干预相关的并发症、EQ-5D-5L 问卷、KOOS 问卷的所有 5 个个体分量表、ACL-QOL 评分、对活动的期望和干预的成本效益。将通过敏感性分析调查主要结局的缺失数据。本文详细介绍了用于分析临床结局的统计分析计划的方法。ACL SNNAP 试验的研究方案以前已经发表过。
本文描述了 ACL SNNAP 试验的分析方法,以最大限度地降低数据驱动结果和报告偏倚的风险。与本文中描述的分析方法的任何偏差都将在试验结果的出版物中进行全面描述和合理说明。
ISRCTN ISRCTN86003324。于 2016 年 11 月 16 日注册。