Actively Recruiting
The Effect of Multimodal Pain Regimen on Use of Narcotics After Rotator Cuff Tear Repair
Led by Montefiore Medical Center · Updated on 2026-01-13
130
Participants Needed
1
Research Sites
45 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to understand which group of pain control medications work best in adults after rotator cuff surgery.
CONDITIONS
Official Title
The Effect of Multimodal Pain Regimen on Use of Narcotics After Rotator Cuff Tear Repair
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults with rotator cuff tears who have failed conservative therapy and are now undergoing arthroscopic rotator cuff repair.
You will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Montefiore Hutchinson Campus
The Bronx, New York, United States, 10461
Actively Recruiting
Research Team
F
Ferdinand Chan, M.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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