FiberLocker® System Augmentation of Rotator Cuff Repairs
NCT: NCT06918041 · RECRUITING
Brief Summary
The purpose of this study is to prospectively evaluate healing, functional clinical outcomes, and safety of arthroscopic rotator cuff repairs augmented with the FiberLocker® System (encompassing the SpeedPatch® PET and the FiberLocker® Instrument). The primary outcome measure is healing evaluation based on Magnetic Resonance Imaging (MRI) at a minimum of 6 months post-operatively. The secondary outcome measures are the Sugaya classification, Goutallier Stage and tendon quality based on MRI as well as objective scores and patient-reported outcome measures (PROMs) from validated outcome scoring systems.
Frequently Asked Questions
What is FiberLocker® System Augmentation of Rotator Cuff Repairs?
FiberLocker® System Augmentation of Rotator Cuff Repairs is a clinical trial registered under NCT06918041. Current status: RECRUITING.
What is the status of NCT06918041?
The current status of NCT06918041 (FiberLocker® System Augmentation of Rotator Cuff Repairs) is: RECRUITING.
When did FiberLocker® System Augmentation of Rotator Cuff Repairs start?
FiberLocker® System Augmentation of Rotator Cuff Repairs started on 2025-08-05.
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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.