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Using ROSA for Challenging The TKA Standard of Care

StatusRecruiting
PhaseNot applicable
Started2024-04-16
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 35 months later Dec 2025 → Dec 2028
See other at-risk trials from London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

Amendment history

2026-09-22
Phase changed: Phase 4 → not applicable
Primary completion pushed: 2025-12 → 2028-12
Completion pushed: 2025-12 → 2028-12
2025-05-09
Study Status v2
Primary completion date2025-04→2025-12
Completion date2025-06→2025-12
2024-04-16
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v1
Trial statusNot Yet Recruiting→Recruiting
Primary completion date2025-01→2025-04
Start dateestimated 2024-02→confirmed 2024-04-16
Study sites0→1
2024-02-12
Original filing
This is a prospective, randomized controlled trial using the cruciate retaining, MC Persona to comparing the conventional TKA to ROSA assisted TKA. Patients will be randomized to one of three study trial arms. 1. Standard of care medial parapetallar approach (Control) 2. ROSA PSA medial parapetallar approach 3. ROSA PSA medial subvastus approach Participants will be followed for 1 year post surgery with a combination of perioperative parameters, imaging, patient reported outcomes, functional outcomes, blood and tissue sampling for inflammatory information and activity levels.
Trial Details
NCT Number NCT06267482
Lead Sponsor London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Collaborators: Zimmer Biomet
Conditions Knee Osteoarthritis
Enrollment 90 participants
Start Date 2024-04-16
Primary Completion 2028-12 (estimated)
Study Completion 2028-12 (estimated)
Updated on ClinicalTrials.gov 2026-09-21