Use of the REGENETEN™ Bioinductive Implant System in High Grade Partial-thickness Tears
← catalyst calendarSponsored by Smith & Nephew, Inc. (industry) · SNN — their whole pipeline →.
Phase
Not applicable
Status
Recruiting
Study type
Interventional
Design
Randomized · Single · Treatment
Enrollment
234estimated
Sites
20
Countries
Australia, Canada, Italy +3
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 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2022-08-30 | actual | When the study began enrolling |
| Primary completion | 2026-08-15 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2028-06-30 | estimated | The whole study's end, after follow-up |
| First posted | 2022-07-06 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-08-05 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Rotator Cuff Injuries
Interventions
- Device: Isolated Bioinductive Repair — also filed as REGENETEN™ Bioinductive Implant
- Procedure: Completion and Repair
Primary outcome
what the primary-completion date above is the date OFChange in Western Ontario Rotator Cuff (WORC)
measured Change from baseline to 3 months post-intervention
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