RecruitingNot ApplicableNCT06729983

Prophylactic Conjoint Tendon Lengthening During Reverse Shoulder Arthroplasty Outcomes

Prophylactic Conjoint Tendon Lengthening During Reverse Shoulder Arthroplasty: is There a Difference in Anterior Shoulder Pain At One Year After Surgery?


Sponsor

Nickolas Garbis

Enrollment

110 participants

Start Date

Mar 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Some patients may experience persistent pain in the front of their shoulder after reverse shoulder replacement. One of the possible reasons for this is that the surgery causes a change in the alignment of the shoulder joint, which may cause increased tension and compression on one of the biceps tendon called the conjoint tendon. The purpose of this study is to evaluate whether conjoint tendon lengthening, a surgical procedure that involves cutting and lengthening the conjoint tendon in order to reduce tension and compression, is able to prevent or reduce the risk of anterior shoulder pain at one year after surgery.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called Prophylactic Conjoint Tendon Lengthening and a procedure called Standard Reverse Shoulder Arthroplasty for people with osteoarthritis shoulder. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREProphylactic Conjoint Tendon Lengthening

During a standard reverse shoulder arthroplasty procedure, the conjoint tendon will be incised and lengthened prophylactically

PROCEDUREStandard Reverse Shoulder Arthroplasty

A standard reverse shoulder arthroplasty procedure will be performed


Locations(1)

Loyola Outpatient Center

Maywood, Illinois, United States

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NCT06729983


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