Clinical Trial

Comparison Between Exactech Guided Personalized Surgery (GPS) and Conventional Instrumentation of Shoulder Arthroplasty

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Summary
The primary objective of this study is to examine the optimization of Reverse Shouder Arthroplasty implant position between GPS and conventional techniques. The secondary objective is to assess the effect of implant position using GPS vs. conventional techniques on ROM and patient reported outcomes. Long-term follow-up to 10 years with minimum 2 year follow-up for patients.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2022-11-07; most recent amendment 2025-02-26.
Trial Details
NCT Number NCT05615259
Lead Sponsor Exactech
Conditions Technology, Comparison
Enrollment 260 participants
Start Date 2020-09-23
Primary Completion 2030-12-31 (estimated)
Study Completion 2031-09-30 (estimated)
Updated on ClinicalTrials.gov 2025-02-28