Clinical Performance and Safety of the Unicompartmental Univation® XF Pro Implant
NCT06657248 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 150
Last updated 2026-05-08
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.
Conditions
- Gonarthritis
- Degenerative Disease
Interventions
- DEVICE
-
univation® XF Pro
Primary medial unicompartmental knee arthroplasty
Sponsors & Collaborators
-
Raylytic GmbH
collaborator INDUSTRY -
Aesculap AG
lead INDUSTRY
Principal Investigators
-
Rolf Haaker, Prof. Dr. · St. Vincenz Hospital Brakel
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-04-02
- Primary Completion
- 2027-10-31
- Completion
- 2032-10-31
Countries
- Germany
Study Locations
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