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Clinical Trial Summary

This is a multi-centre, single cohort trial of patients undergoing cruciate-retaining total knee arthroplasty with the Attune Cementless, Fixed Bearing, Cruciate Retaining TKA System.


Clinical Trial Description

All patients will undergo post-operative radiostereometric analysis (RSA) and computed tomography (CT) to quantify and characterize the in vivo migration pattern of the Attune AFFIXIUM Cementless Tibial Baseplate and the Attune POROCOAT Cementless Femoral Component up to 24 months. Patient health and functional outcomes will be recorded at pre- and post-operative intervals for all patients. Peri-operative adverse events and other clinical complications will be captured as encountered. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06189872
Study type Interventional
Source Canadian Radiostereometric Analysis Network
Contact Sarah Tran
Phone 204-926-1231
Email stran@orthoinno.com
Status Not yet recruiting
Phase N/A
Start date March 2024
Completion date June 2027

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