Evaluation Of Outcomes Following Rotator Cuff Repair Using the REGENETEN Bioinductive Implant
NCT: NCT06857084 · RECRUITING
Brief Summary
This prospective, single-arm, multicenter registry is being conducted to collect real world post-market data from patients who are undergoing rotator cuff repair using the REGENETEN◊ Bioinductive Implant System. The Registry will include up to 50 centers in the United Kingdom (UK), Europe, Australia, and up to 400 patients for the initial evaluation. Patients will be treated and evaluated according to standard medical care. Outcome data is collected up to 2 years post-surgery.
Frequently Asked Questions
What is Evaluation Of Outcomes Following Rotator Cuff Repair Using the REGENETEN Bioinductive Implant?
Evaluation Of Outcomes Following Rotator Cuff Repair Using the REGENETEN Bioinductive Implant is a clinical trial registered under NCT06857084. Current status: RECRUITING.
What is the status of NCT06857084?
The current status of NCT06857084 (Evaluation Of Outcomes Following Rotator Cuff Repair Using the REGENETEN Bioinductive Implant) is: RECRUITING.
When did Evaluation Of Outcomes Following Rotator Cuff Repair Using the REGENETEN Bioinductive Implant start?
Evaluation Of Outcomes Following Rotator Cuff Repair Using the REGENETEN Bioinductive Implant started on 2020-10-01.
Related Devices
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.