Clin2
NCT06857084Likely a fitRecruiting

Rotator cuff repair with REGENETEN implant study

Rotator Cuff Injuries

Part of Injuries & trauma clinical trials.

This study tracks how well patients recover after rotator cuff repair surgery using the REGENETEN bioinductive implant. It aims to see if the implant helps improve healing and outcomes.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
400 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You need to have a rotator cuff tear (partial or full) that requires arthroscopic surgery.
  • You must be 18 years or older at the time you agree to participate.
  • You should not have any emotional or mental health condition that makes it hard for you to take part, like severe mental illness or problems with drugs or alcohol.
  • You must be suitable for the REGENETEN implant according to its instructions for use.
  • You cannot be considered a vulnerable person as defined by research standards.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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