Condition: Rotator Cuff Tears · Sponsor: Spital Thurgau AG
This single-center, prospective, randomized controlled study will compare patients allocated to two treatment arms who are undergoing surgery to repair rotator cuff tears: (1) arthroscopic rotator cuff reconstruction using fixation with anchors augmented with a synthetic polyester patch, and (2) arthroscopic rotator cuff reconstruction using fixation with anchors and no augmentation with a synthetic polyester patch. The primary objective is to compare complications (primarily retear rates) and the secondary objective is to compare mid- and long-term clinical and radiological outcomes using standard orthopedic assessments, such as the subjective shoulder value and the Constant-Murley score.
This description comes directly from the study's public registry record.
Florian Hess, MD · +41 58 144 8143 · florian.hess@stgag.ch
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| Spital Thurgau AG | Frauenfeld, Thurgau, Switzerland | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06076902