NCT07076069 The Effect of Multimodal Pain Regimen on Use of Narcotics After Rotator Cuff Tear Repair
| NCT ID | NCT07076069 |
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Montefiore Medical Center |
| Condition | Rotator Cuff Repairs |
| Study Type | INTERVENTIONAL |
| Enrollment | 130 participants |
| Start Date | 2025-07-21 |
| Primary Completion | 2026-06-01 |
Trial Parameters
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Brief Summary
The goal of this clinical trial is to understand which group of pain control medications work best in adults after rotator cuff surgery.
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