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CRISTAL (a cluster-randomised, crossover, non-inferiority trial of aspirin compared to low molecular weight heparin for venous thromboembolism prophylaxis in hip or knee arthroplasty, a registry nested study): statistical analysis plan.

Authors :
Sidhu, Verinder Singh
Kelly, Thu-Lan
Pratt, Nicole
Graves, Steven
Buchbinder, Rachelle
Naylor, Justine
de Steiger, Richard
Ackerman, Ilana
Adie, Sam
Lorimer, Michelle
Bastiras, Durga
Cashman, Kara
Harris, Ian
Source :
Trials; 8/24/2021, Vol. 22 Issue 1, p1-14, 14p, 1 Illustration, 2 Diagrams, 5 Charts, 1 Graph
Publication Year :
2021

Abstract

<bold>Background: </bold>This a priori statistical analysis plan describes the analysis for CRISTAL.<bold>Methods: </bold>CRISTAL (cluster-randomised, crossover, non-inferiority trial of aspirin compared to low molecular weight heparin for venous thromboembolism prophylaxis in hip or knee arthroplasty, a registry nested study) aims to determine whether aspirin is non-inferior to low molecular weight heparin (LMWH) in preventing symptomatic venous thromboembolism (VTE) following hip arthroplasty (HA) or knee arthroplasty (KA). The study is nested within the Australian Orthopaedic Association National Joint Replacement Registry. The trial was commenced in April 2019 and after an unplanned interim analysis, recruitment was stopped (December 2020), as the stopping rule was met for the primary outcome. The clusters comprised hospitals performing > 250 HA and/or KA procedures per annum, whereby all adults (> 18 years) undergoing HA or KA were recruited. Each hospital was randomised to commence with aspirin, orally, 85-150 mg daily or LMWH (enoxaparin), 40 mg, subcutaneously, daily within 24 h postoperatively, for 35 days after HA and 14 days after KA. Crossover was planned once the registration target was met for the first arm. The primary end point is symptomatic VTE within 90 days. Secondary outcomes include readmission, reoperation, major bleeding and death within 90 days, and reoperation and patient-reported pain, function and health status at 6 months. The main analyses will focus on the primary and secondary outcomes for patients undergoing elective primary total HA and KA for osteoarthritis. The analysis will use an intention-to-treat approach with cluster summary methods to compare treatment arms. As the trial stopped early, analyses will account for incomplete cluster crossover and unequal cluster sizes.<bold>Conclusions: </bold>This paper provides a detailed statistical analysis plan for CRISTAL.<bold>Trial Registration: </bold>Australian and New Zealand Clinical Trials Registry ACTRN12618001879257 . Registered on 19/11/2018. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17456215
Volume :
22
Issue :
1
Database :
Complementary Index
Journal :
Trials
Publication Type :
Academic Journal
Accession number :
152057483
Full Text :
https://doi.org/10.1186/s13063-021-05486-0