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Study identifier: NCT05966519 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

ROSA Knee Intraoperative Planning Flexibility Study

Condition: Osteo Arthritis Knee · Rheumatoid Arthritis  ·  Sponsor: Zimmer Biomet

PhaseN/A
Planned participants80
Who can joinAll sexes, 20 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Noriko Sugawara  ·  +81-3-6402-6600  ·  noriko.sugawara@zimmerbiomet.com

Always discuss trial participation with your own doctor first.

Locations (1)

Kyushu University HospitalFukuoka, Fukuoka, JapanRecruiting

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Source record: clinicaltrials.gov/study/NCT05966519