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The Effect of Multimodal Pain Regimen on Use of Narcotics After Rotator Cuff Tear Repair
RecruitingPhase 4
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Inclusion Criteria: * Adults with rotator cuff tears who have failed conservative therapy and are now undergoing arthroscopic rotator cuff repair. Exclusion Criteria: * 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
About the study
The goal of this clinical trial is to understand which group of pain control medications work best in adults after rotator cuff surgery.
What is being tested
- Multimodal Pain Regimen (drug)
- Standard of Care Pain Regimen (drug)
Sponsor: Montefiore Medical Center · Participants: 130 · Started: Jul 21, 2025
Contact the study team
- Ferdinand Chan, M.D. · Phone: 718-920-2060
Official record on ClinicalTrials.gov — NCT07076069
Locations in the U.S.
| New York | Montefiore Hutchinson Campus, The Bronx |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.