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RECRUITING
NCT07005063
NA

Rotator Cuff Tendon Repair With FiberLocker System Patch Augmentation

Sponsor: ZuriMED Technologies AG

View on ClinicalTrials.gov

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.

Official title: Rotator Cuff Tendon Repair With FiberLocker System Patch Augmentation: A Prospective, Single-Arm, Non-Randomized, Pilot Study

Key Details

Gender

All

Age Range

40 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

50

Start Date

2025-07-03

Completion Date

2029-06-30

Last Updated

2025-07-17

Healthy Volunteers

No

Interventions

DEVICE

FiberLocker® System (encompassing SpeedPatch® PET and FiberLocker Instrument® SN)

The FiberLocker® System is a mechanical augmentation system that includes an implant (SpeedPatch® PET) and an instrument (FiberLocker® Instrument SN) for its attachment. The implant is composed of non-woven PET fibers, and the instrument features a reciprocating needle at its tip, which pushes the individual patch fibers into the underlying tendon tissue

Locations (1)

Balgrist University Hospital

Zurich, Canton of Zurich, Switzerland