RecruitingPhase 4NCT07076069

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

Sponsor

Montefiore Medical Center

Enrollment

130 participants

Start Date

Jul 21, 2025

Study Type

INTERVENTIONAL

Conditions

Pain Management Rotator Cuff Repairs

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

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Multimodal Pain Regimen and a drug called Standard of Care Pain Regimen for people with pain management and rotator cuff repairs. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGMultimodal Pain Regimen

Preoperatively: One dose of Pregabalin 100mg and Celecoxib 400mg along with interscalene block Intraoperatively: Intravenous Dexamethasone 0.1mg/kg (maximum dose of 8mg), Magnesium 2g, Acetaminophen 1000mg, and local infiltration of 0.5% Ropivacaine 20ml Postoperatively (Discharge): Acetaminophen 975mg every 4 hours, Meloxicam 7.5mg once per day, Pregabalin 50mg twice per day, Magnesium 400mg once per day, along with rescue Oxycodone 5mg every 4 hours, as needed

DRUGStandard of Care Pain Regimen

No preoperative medications. Interscalene block in the preoperative holding area. Alternating Acetaminophen 975mg and Ibuprofen 600mg every 4 hours, with rescue Oxycodone 5mg every 4 hours, as needed