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A Study Comparing Shoulder Replacement Techniques For Patients With Shoulder Arthritis And An Intact Rotator Cuff

RECRUITINGN/ASponsored by Mayo Clinic
Actively Recruiting
PhaseN/A
SponsorMayo Clinic
Started2026-05-05
Est. completion2029-07
Eligibility
Age60 Years – 85 Years
Healthy vol.Accepted
Locations1 site
View on ClinicalTrials.gov →

NCT07584356

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

Age: 60 Years – 85 YearsHealthy volunteers accepted
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

Conditions2

ArthritisShoulder Arthritis

Locations1 site

Mayo Clinic in Rochester
Rochester, Minnesota, 55905
Lucille I Anderson, CCRP507-538-5627anderson.luci@mayo.edu

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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

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