MISHA Post-Market Clinical Study
Start Date
11/3/2023
Completion Date
7/30/2030
Summary
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.
Eligibility Criteria
Age Range: 25 years to 65 years
Interventions
MISHA Knee System
Conditions
Locations
Weiss Orthopedics
Sonoma, California 95476
United States
Orthopaedics Specialists of NC
Raleigh, North Carolina 27614
United States
Oregon Health and Science University
Portland, Oregon 97239
United States
University of Virginia
Charlottesville, Virginia 22903
United States