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The goal of this clinical trial is to understand which group of pain control medications work best in adults after rotator cuff surgery.
The purpose of this study is to investigate whether a previously described multimodal pain protocol involving non-narcotic medications compared to the medical center's current postoperative pain regimen mainly involving narcotics will decrease total rescue narcotics used for patients who undergo arthroscopic rotator cuff tear repair at Montefiore. The implications of the study would be reduced narcotics consumptions in postoperative patients and improved self-reported patient outcomes. Through this study, the investigator team hopes to develop a pain regimen that alleviates dependence on opioids in postoperative patients without sacrificing patient satisfaction and comfort.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Montefiore Hutchinson Campus
The Bronx, New York, United States
Start Date
July 21, 2025
Primary Completion Date
June 1, 2026
Completion Date
June 1, 2026
Last Updated
January 13, 2026
130
ESTIMATED participants
Multimodal Pain Regimen
DRUG
Standard of Care Pain Regimen
DRUG
Lead Sponsor
Montefiore Medical Center
NCT07327463
NCT07432711
Data Source & Attribution
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