ORIGIN® vs. VANGUARD® PS Observational Study

Recruiting Observational Study
Arthroplasty Replacement Knee
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
140 (estimated)
Sponsor
Symbios Orthopedie SA · Industry
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About This Trial

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.

Trial Locations
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Eligibility Criteria
Inclusion/exclusion criteria
Contacts

Lukas Eckhard

+496131177302

lukas.eckhard@unimedizin-mainz.de

CONTACT