MISHA Post-Market Clinical Study
Recruiting now · Not applicable
Conditions studied: Osteo Arthritis Knee
In brief
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.
Key facts
- Study ID
- NCT06118892
- Run by
- Moximed
- People needed
- 120
- Starts
- 2023-11-03
- Expected to finish
- 2030-07-30
- Last updated by the study team
- 2026-07-14
Who can join
Age: 25 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Weiss Orthopedics — Sonoma, California, United States (enrolling)
- Orthopaedics Specialists of NC — Raleigh, North Carolina, United States (enrolling)
- Oregon Health and Science University — Portland, Oregon, United States (enrolling)
- University of Virginia — Charlottesville, Virginia, United States (enrolling)
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.