PMCF Study on the Safety, Performance and Clinical Benefits Data of the ComposiTCP
Recruiting
Observational Study
Rotator Cuff Repairs
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 43 (estimated)
- Sponsor
- Zimmer Biomet · Industry
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About This Trial
The study is a multicenter, retrospective and prospective, non-randomized, noncontrolled, and consecutive series post-market study. The purpose of this study is collect data confirming safety, performance and clinical benefits of the ComposiTCP Suture Anchors Double Loaded with BroadBand Tape, Sliding implants when used in rotator cuff repair.
The primary endpoint of this study is the assessment …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Subject was treated with the ComposiTCP Suture Anchors Double Loaded with BroadBand Tape, Sliding for rotator cuff repair;
* At least 18 years old and skeletally mature;
* Willing and able to comply with the study procedures;
* Subject is capable of understanding the doctor's …
Contacts