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Clinical Trial

Embody Post-Market Clinical Follow-Up Study

NCT: NCT05735119 · ACTIVE_NOT_RECRUITING

NCT IDNCT05735119
StatusACTIVE_NOT_RECRUITING
Start Date2022-11-09
SponsorZimmer Biomet (INDUSTRY)
First posted
Last updated

Brief Summary

A multi-center, prospective post-market clinical follow-up study: subscapularis repair augmented with Tapestry Biointegrative Implant after shoulder arthroplasty. The primary objective of this study is to evaluate the long-term integrity of the subscapularis tendon repair after shoulder arthroplasty augmented with Tapestry Biointegrative Implant, assessed by ultrasound 6 months postoperatively. Secondary objectives are to assess shoulder function (internal rotation strength), safety, and patient reported outcomes. Patients will be evaluated preoperatively, at the time of surgery, 3, 6, 12 and 24 months after surgery.

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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