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Recruiting NCT07584356

NCT07584356 A Study Comparing Shoulder Replacement Techniques For Patients With Shoulder Arthritis And An Intact Rotator Cuff

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Clinical Trial Summary
NCT ID NCT07584356
Status Recruiting
Phase
Sponsor Mayo Clinic
Condition Shoulder Arthritis
Study Type INTERVENTIONAL
Enrollment 108 participants
Start Date 2026-05-05
Primary Completion 2029-07

Eligibility & Interventions

Sex All sexes
Min Age 60 Years
Max Age 85 Years
Study Type INTERVENTIONAL
Interventions
aTSArTSA

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 108 participants in total. It began in 2026-05-05 with a primary completion date of 2029-07.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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

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

Contact & Investigator

Central Contact

Lucille I Anderson, CCRP

✉ anderson.luci@mayo.edu

📞 507-538-5627

Principal Investigator

Jonathan D. Barlow, MD

PRINCIPAL INVESTIGATOR

Mayo Clinic

Frequently Asked Questions

Who can join the NCT07584356 clinical trial?

This trial is open to participants of all sexes, aged 60 Years or older, up to 85 Years, studying Shoulder Arthritis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07584356 currently recruiting?

Yes, NCT07584356 is actively recruiting participants. Contact the research team at anderson.luci@mayo.edu for enrollment information.

Where is the NCT07584356 trial being conducted?

This trial is being conducted at Rochester, United States.

Who is sponsoring the NCT07584356 clinical trial?

NCT07584356 is sponsored by Mayo Clinic. The principal investigator is Jonathan D. Barlow, MD at Mayo Clinic. The trial plans to enroll 108 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology