NCT07584356NARecruiting
A Study Comparing Shoulder Replacement Techniques For Patients With Shoulder Arthritis And An Intact Rotator Cuff
Mayo Clinic
Start Date
5/5/2026
Completion Date
12/1/2029
Summary
The purpose of this study is to determine if patients undergoing anatomic total shoulder arthroplasty (aTSA) will have improved patient reported outcome scores at 1 year compared to those undergoing reverse total shoulder arthroplasty (rTSA).
Eligibility Criteria
Age Range: 60 years to 85 years
Inclusion Criteria
* Shoulder arthritis
* Intact rotator cuff
* Glenoid retroversion less than 25°
Exclusion Criteria
* Rotator cuff insufficiency
* Fracture deformity/sequelae
* Severe glenoid deformity (C glenoid, severe A2, B2 glenoid)
* Current or previous infection of shoulder
* Previous acromion fracture (not os acromiale)
* Brachial plexopathy
* Axillary neuropathy
* Current drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements.
* Inability or unwillingness of individual or legal guardian/representative to give written informed consent.
* Medical conditions that would make 2 years follow up unlikely
* Non-English speaking
Interventions
PROCEDURE
aTSA
PROCEDURE
rTSA
Conditions
Shoulder Arthritis
Locations
Mayo Clinic in Rochester
Rochester, Minnesota 55905
United States