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Recruiting NCT07076069

The Effect of Multimodal Pain Regimen on Use of Narcotics After Rotator Cuff Tear Repair

Conditions: Rotator Cuff Repairs, Pain Management

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: PHASE4
Enrollment: 130
Sponsor: Montefiore Medical Center

Location: Montefiore Hutchinson Campus The Bronx New York

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

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07076069). StuddyBuddy aggregates publicly available trial information.