This registry is designed to collect information on how different surgical procedures are used and how well they work in treating knee cartilage damage. Information will be collected from patients undergoing knee surgery for cartilage damage and entered into a large database that reflects routine clinical practice ("real-world" data). The data collected will be used to support future research and improve understanding of treatment outcomes for knee cartilage repair.
The registry will collect both prospective and retrospective/prospective data.
Study Type
OBSERVATIONAL
Enrollment
1,000
Marketed Product - MP01 is a medical device used in the treatment of knee-joint surface lesions.
Any other surgical procedures used in the treatment of knee-joint surface lesions that fall within the Marketed Product - MP01 on label indication.
CAO Research Foundation
Washington D.C., District of Columbia, United States
The Orthopaedic Research Foundation, Inc.
Indianapolis, Indiana, United States
Oklahoma Sports Science and Orthopedics
Oklahoma City, Oklahoma, United States
International Knee Documentation Committee (IKDC) Subjective Knee Evaluation Score change from Baseline to 24-months
The IKDC Subjective Knee Evaluation Form assesses the subject's opinion of their knee across 3 domains: symptoms (7 items), sports activity (2 items), and knee function (2 items; note: 'function prior to knee injury' is not included in the overall score). Responses vary for each item. The sum of all items is converted to a scale of 0 to 100, where 100 represents no limitation with activities \& absence of symptoms (i.e., the best outcome) and 0 represents the worst outcome.
Time frame: Baseline and 24 months
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