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Clinical Trial

FiberLocker® System Augmentation of Rotator Cuff Repairs

NCT: NCT06918041 · RECRUITING

NCT IDNCT06918041
StatusRECRUITING
Start Date2025-08-05
Completion2028-04-01
SponsorZuriMED Technologies Inc. (INDUSTRY)
First posted
Last updated

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.

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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