The Effect of Multimodal Pain Regimen on Use of Narcotics After Rotator Cuff Tear Repair
Recruiting now · Phase 4
Conditions studied: Rotator Cuff Repairs, Pain Management
In brief
The goal of this clinical trial is to understand which group of pain control medications work best in adults after rotator cuff surgery.
Key facts
- Study ID
- NCT07076069
- Run by
- Montefiore Medical Center
- People needed
- 130
- Starts
- 2025-07-21
- Expected to finish
- 2028-06-01
- Last updated by the study team
- 2026-07-13
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults with rotator cuff tears who have failed conservative therapy and are now undergoing arthroscopic rotator cuff repair.
You may not qualify if…
- Patients without capacity to consent for the study
- Patients not able to have local nerve block
- Patients who underwent previous shoulder surgery on the same side, kindling revision rotator cuff repair
- Patients who are unable to record and verbalize their pain level due to altered mental status
- Patients who are unable to tolerate any of the medications included in the multimodal pain regimen or standard pain regimen due to severe allergies or inability to consume medication
- Patients with history of previously diagnosed alcohol or drug abuse, renal impairment, peptic ulcer disease, and gastrointestinal bleeding
- Patients who are pregnant
Where it is running
- Montefiore Hutchinson Campus — The Bronx, New York, United States (enrolling)
Full record on ClinicalTrials.gov
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