Patient Outcomes Following Kinematic and Functional Alignment in Robotic-Assisted Total Knee Arthroplasty With Randomized Insert Types

Summary

This study aims to evaluate patient outcomes following robotic-assisted total knee arthroplasty using the VELYS system. Patients undergoing surgery will receive either kinematic alignment or functional alignment as determined by the operating surgeon as part of routine clinical care. Within each surgical technique group, patients will be randomly assigned to receive different implant insert types (medial stabilised or cruciate retaining) using a REDCap-based randomisation process. Patient-reported outcome measures will be collected before surgery and at follow-up time points after surgery to assess clinical outcomes.

Eligibility

\*Inclusion Criteria:\*

* Patients undergoing robotic-assisted total knee arthroplasty using the VELYS system
* Diagnosis of knee osteoarthritis requiring surgical intervention
* Able to provide informed consent
* Willing to complete patient-reported outcome measures

\*\*Exclusion Criteria:\*\*

* Patients undergoing revision knee arthroplasty
* Presence of active infection
* Inability to comply with follow-up assessments
* Severe co-morbidities that may affect surgical outcomes or participation in the study

Conditions3

Browse More Trials