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Clinical Trial Summary

The objective of the study is a multi-center prospective registry to collect clinical outcomes of anatomic and reverse total shoulder arthroplasty.


Clinical Trial Description

The study is a non-randomized multi-center prospective registry and subjects will be treated according to standard of care at each center. Subjects will be approached for participation in this study after they have made the decision to undergo a primary or revision shoulder arthroplasty procedure. The treating surgeon will obtain verbal consent from the patient for a research coordinator to screen for eligibility. Patients who meet all criteria will be offered enrollment into the study. The total enrollment goal is a minimum of 500 anatomic shoulder arthroplasty and 500 reverse shoulder arthroplasty subjects enrolled in the multi-center registry. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03511586
Study type Observational [Patient Registry]
Source Arthrex, Inc.
Contact Kelly Ganz, BA, CCRC
Phone 1 (800) 933-7001
Email kelly.ganz@arthrex.com
Status Recruiting
Phase
Start date July 28, 2015
Completion date November 10, 2027

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