This study will evaluate the clinical performance of DePuy Global® AP™ Shoulder prosthesis using the anchor pegged glenoid component and clinical and radiographic evaluations.
The purpose of the study is to determine the difference between pre-operative and post-operative levels of patient satisfaction, shoulder function, radiographic alignment, shoulder pain and patient satisfaction in patients receiving a Global® AP™ shoulder prosthesis for glenohumeral arthritis.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
64
Total shoulder arthroplasty
The CORE Institute
Phoenix, Arizona, United States
Mission Hospitals Research Institute
Asheville, North Carolina, United States
Wellington Orthopaedics and Sports Medicine
Cincinnati, Ohio, United States
Rosenberg Cooley Metcalf Clinic
Park City, Utah, United States
Constant Shoulder Score
Time frame: Pre-op, 6, 12, 24 months
SF-12
Time frame: Pre-op, 6,12, 24 months
Penn/ASES
Time frame: Pre-Op, 6, 12, and 24 months
Radiographic Data
Time frame: Pre-Op, 6 weeks, 6, 12, and 24 months
Quality of Life Survey
Time frame: 6 weeks
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