Clinical Trial

Clinical Performance and Safety of the Unicompartmental Univation® XF Pro Implant

Study acronym: UNI_XF_PRO
Recruiting
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Summary
The study is designed as a prospective, observational, mid-term, multi-center follow-up study. It is planned to include 150 patients from 4 different study centres in Germany.
Protocol Amendment History 1 change
critical Recruitment opened 2026-05-09
Trial Details
NCT Number NCT06657248
Lead Sponsor Aesculap AG
Collaborators: Raylytic GmbH
Conditions Gonarthritis, Degenerative Disease
Enrollment 150 participants
Start Date 2026-04-02
Primary Completion 2027-10 (estimated)
Study Completion 2032-10 (estimated)
Updated on ClinicalTrials.gov 2026-05-08