Rotator Cuff Tendon Repair With FiberLocker System Patch Augmentation
NCT: NCT07005063 · RECRUITING
Brief Summary
The overall objective of this clinical investigation is to assess the safety and efficacy of full-thickness arthroscopic rotator cuff repairs augmented with the FiberLocker System for the subjects. The primary outcome of the investigation is to assess the safety after full-thickness arthroscopic rotator cuff repairs augmented with the FiberLocker System in terms of postoperative adverse events through the 12-month follow-up. Main secondary outcomes include measures of efficacy and clinical performance evaluated at 6-week, 4.5-month, and 12-month follow-ups including retear rate assessed using MRI and different functional performance scores.
Frequently Asked Questions
What is Rotator Cuff Tendon Repair With FiberLocker System Patch Augmentation?
Rotator Cuff Tendon Repair With FiberLocker System Patch Augmentation is a clinical trial registered under NCT07005063. Current status: RECRUITING.
What is the status of NCT07005063?
The current status of NCT07005063 (Rotator Cuff Tendon Repair With FiberLocker System Patch Augmentation) is: RECRUITING.
When did Rotator Cuff Tendon Repair With FiberLocker System Patch Augmentation start?
Rotator Cuff Tendon Repair With FiberLocker System Patch Augmentation started on 2025-07-03.
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Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.