Condition: Osteo Arthritis Knee · Sponsor: Moximed
Prospective evaluation of the safety and effectiveness of the MISHA Knee System. The study will collect data on the procedural and long-term adverse events, WOMAC pain and function scores, KSS satisfaction, subsequent surgical interventions, BMI levels, range of motion, UCLA activity level of the subjects, and perform radiographic/x-ray evaluations at clinical visits through 5 years post-procedure. The primary analysis of this study is freedom from device- and procedure-related SSIs at five (5) years post-implantation. This study will also assess device performance in subjects with intact and retained devices and subjects with devices removed prior to study termination and freedom from conversion to arthroplasty through 5 years. Study subjects will be followed over a five-year post-implant period.
This description comes directly from the study's public registry record.
Rose Weinstein · (510) 887 3375 · rsweinstein@moximed.com
Always discuss trial participation with your own doctor first.
| Weiss Orthopedics | Sonoma, California, United States | Recruiting |
| Orthopaedics Specialists of NC | Raleigh, North Carolina, United States | Recruiting |
| Oregon Health and Science University | Portland, Oregon, United States | Recruiting |
| University of Virginia | Charlottesville, Virginia, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06118892