ROSA Knee Intraoperative Planning Flexibility Study
NCT: NCT05966519 · RECRUITING
Brief Summary
The purpose of this study is to verify that an orthopedic surgical assist robot (ROSA Knee System) can provide intraoperative adjustment of osteotomy angle and volume for total knee arthroplasty (TKA) based on feedbacks obtained from intraoperative soft tissue conditions. A total 80 cases will be enrolled at one study site with a postoperative follow-up period of 2 years.
Frequently Asked Questions
What is ROSA Knee Intraoperative Planning Flexibility Study?
ROSA Knee Intraoperative Planning Flexibility Study is a clinical trial registered under NCT05966519. Current status: RECRUITING.
What is the status of NCT05966519?
The current status of NCT05966519 (ROSA Knee Intraoperative Planning Flexibility Study) is: RECRUITING.
When did ROSA Knee Intraoperative Planning Flexibility Study start?
ROSA Knee Intraoperative Planning Flexibility Study started on 2024-01-05.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.