Actively Recruiting
Multi-Center Registry for Anatomic and Reverse Total Shoulder Arthroplasty Procedures
Led by Arthrex, Inc. · Updated on 2025-08-11
2500
Participants Needed
24
Research Sites
17 weeks
Total Duration
AI-Summary
What this Trial Is About
This research aims to collect clinical outcomes from patients undergoing anatomic or reverse total shoulder arthroplasty. It is a multi-center prospective registry focusing on patients who have decided to have either a primary or revision shoulder replacement surgery. The study is designed to gather data over time to better understand patient experiences and results after these procedures. Participants will receive shoulder arthroplasty treatment based on the usual care at each participating center. The study plans to enroll at least 500 subjects receiving anatomic shoulder replacements and 500 receiving reverse shoulder replacements. There is no randomization or experimental treatment involved instead, the registry records outcomes following standard surgical procedures. During the study, patients will be asked to fill out questionnaires and attend follow-up visits to monitor their progress and recovery. Preoperative CT scans will be used for surgical planning, and participants will comply with prescribed physical therapy after surgery. The main outcome measured is the change in pain over a 10-year period, helping researchers understand long-term effects. Participants will be monitored throughout their recovery and beyond as part of the registry.
CONDITIONS
Brief Title
Total Shoulder Arthroplasty Multi-Center Registry
Research Team
K
Kelly Ganz, BA, CCRC
A
Alicia Ruiz, MS, CCRP, CCRA
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