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Study identifier: NCT07138898 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Immunosuppressant Management in Rheumatology Patients Undergoing Elective Total Shoulder Arthroplasty

Condition: Rheumatic Disease  ·  Sponsor: NYU Langone Health

PhasePhase 2
Planned participants80
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to assess the incidence of rheumatologic flares, changes in pain scores (VAS), changes in functional outcomes (PROMIS), wound complications, surgical site infections, and return trips to the operating room for rheumatology patients following shoulder replacements, comparing those who stop their immunosuppressants preoperatively for the same amount of time as suggested in the literature for hip and knee arthroplasty versus those who hold the medications for a shorter period of time preoperatively.

This description comes directly from the study's public registry record.

Talk to the study team

Thomas Chalothron  ·  646-501-7384  ·  Thomas.Chalothron@nyulangone.org

Vinay Bijoor  ·  914-610-6112  ·  Vinay.Bijoor@nyulangone.org

Always discuss trial participation with your own doctor first.

Locations (1)

NYU Langone HealthNew York, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07138898