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Clinical Trial

ROSA Knee Intraoperative Planning Flexibility Study

NCT: NCT05966519 · RECRUITING

NCT IDNCT05966519
StatusRECRUITING
Start Date2024-01-05

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.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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