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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

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Conditions

Shoulder Arthritis

Locations

Mayo Clinic in Rochester

Rochester, Minnesota 55905

United States