Condition: Knee Arthropathy · Recurrence · Knee Infection · Sponsor: The Cleveland Clinic
This study is a prospectively and retrospectively enrolled, post-market, open-label, non-randomized, single institution evaluation of clinical outcomes of primary or revision knee surgery patients who meet the eligibility criteria and received devices from the Triathlon Hinge Knee System according to its indications for use (IFU). Clinical evaluation for all cases will include data collection of patient demographics, surgical details, early postoperative status, functional and clinical outcomes, and survivorship at 1, 2, 6, and 10-years.
This description comes directly from the study's public registry record.
Laura Stiegel · 216-442-5511 · stiegel@ccf.org
Sanal Krishnan, PHD · 216-445-7194 · krishns11@ccf.org
Always discuss trial participation with your own doctor first.
| Cleveland Clinic Florida | Weston, Florida, United States | Recruiting |
| Cleveland Clinic | Cleveland, Ohio, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06379321