Knee Cartilage Repair Registry

Part of paid clinical trials in Washington D.C., District of Columbia.

Sponsor
Smith & Nephew, Inc.
Study ID
NCT07786207
Status
Not Yet Recruiting

Notify me when recruiting opens

Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.

Not yet recruiting

Add your contact details and location so we can keep your interest tied to this study.

Conditions

  • Joint Surface Knee Lesions
  • Knee Injuries

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Marketed Product - MP01 — DEVICE
    Marketed Product - MP01 is a medical device used in the treatment of knee-joint surface lesions.
  • Other Surgical Treatments — PROCEDURE
    Any other surgical procedures used in the treatment of knee-joint surface lesions that fall within the Marketed Product - MP01 on label indication.

Study Details

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.

Key Dates

First listed
Aug 25, 2026
Start date
Sep 30, 2026
Status verified
Jun 2026
Primary completion
Mar 31, 2034
Completion
Mar 31, 2034

Study Design

Enrollment
1,000 participants (estimated)

Arms

  • Arm: Marketed Product - MP01
    Participants who are having knee cartilage surgery with Marketed Product - MP01
  • Arm: Other Knee Cartilage Procedures
    Participants who are having knee cartilage surgery with a procedure other than using Marketed Product - MP01

Primary Outcome Measure

International Knee Documentation Committee (IKDC) Subjective Knee Evaluation Score change from Baseline to 24-months [ Time Frame: Baseline and 24 months ]

Central Contacts

Locations (3)

FacilityCityStateZIPSite coordinators
CAO Research FoundationWashington D.C.District of Columbia20036
Scott Faucett, MD, MS (PRINCIPAL_INVESTIGATOR)
The Orthopaedic Research Foundation, Inc.IndianapolisIndiana46278
Melanie Glover
[email protected]
Corey Kendall, MD (PRINCIPAL_INVESTIGATOR)
Oklahoma Sports Science and OrthopedicsOklahoma CityOklahoma73114
Elaine Justice
[email protected]
R. Garrett Steinmetz, MD (PRINCIPAL_INVESTIGATOR)

Find similar trials in Washington D.C., DC

By research site
CAO Research Foundation· Washington D.C., DCThe Orthopaedic Research Foundation, Inc.· Indianapolis, INOklahoma Sports Science and Orthopedics· Oklahoma City, OK

Related Studies