ORIGIN® vs. VANGUARD® PS Observational Study
Recruiting now
Conditions studied: Arthroplasty, Replacement, Knee
In brief
The study objective is to assess patient satisfaction after the surgery with a patient match CE marked implant (ORIGIN®) versus off-the-shelf (VANGUARD PS) device, and to document the clinical and device performance outcomes of the ORIGIN System used in routine hospital practice in a large patient cohort treatment of total knee arthroplasty.
Key facts
- Study ID
- NCT04728542
- Run by
- Symbios Orthopedie SA
- People needed
- 140
- Starts
- 2021-03-25
- Expected to finish
- 2027-02-01
- Last updated by the study team
- 2024-10-04
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- University Medical Center of Johannes Gutenberg-University Mainz — Mainz, Germany (enrolling)
Full record on ClinicalTrials.gov
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