Knee Cartilage Repair Registry
← catalyst calendarNCT07786207 · readout in 2,774 d
Sponsored by Smith & Nephew, Inc. (industry) · SNN — their whole pipeline →.
Phase
—
Status
Not yet recruiting
Study type
Observational
Enrollment
1,000estimated
Sites
3
Country
United States
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-25
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2026-09-30 | estimated | When the study began enrolling |
| Primary completion | 2034-03-31 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2034-03-31 | estimated | The whole study's end, after follow-up |
| First posted | 2026-08-25 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-08-25 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Conditions
- Knee Injuries
- Joint Surface Knee Lesions
Interventions
- Device: Marketed Product - MP01
- Procedure: Other Surgical Treatments
Primary outcome
what the primary-completion date above is the date OFInternational Knee Documentation Committee (IKDC) Subjective Knee Evaluation Score change from Baseline to 24-months
measured Baseline and 24 months
Related
SNN · their whole pipeline · Congress trades in SNN
SNN's other studiesmost recently updated first
- A Global Clinical Study Investigating the Safety and Effectiveness of Smith and Nephew's Porous Knee System in Patients Who Need a Total Knee Replacement Due to Degenerative Arthritis, Post-traumatic Arthritis or Inflammatory Arthritis — · Active, not recruiting
- A Multi-Center Study Assessing the Safety and Efficacy of the LEGION Medial Stabilized (MS) Insert in Patients Undergoing a Total Knee Arthroplasty (TKA) — · Recruiting
- Use of the REGENETEN™ Bioinductive Implant System in High Grade Partial-thickness Tears Not applicable · Recruiting
- A Post Approval Multicenter 10 Year Follow-up Observational Trial of Marketed Product - MP01 vs. Surgical Standard of Care (SSOC) Used for the Treatment of Joint Surface Lesions of the Knee — · Enrolling by invitation
- Safety and Performance of MICRORAPTOR™ Suture Anchors in Shoulder and Hip — · Completed
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