drugset / Trial / NCT07227064

Methadone in THA for Post-op Pain and Opioid Reduction

NCT07227064

Phase 3 Recruiting 162 enrolled Medical University of South Carolina
RandomizedParallel-groupDouble-blindTreatment

Summary

This randomized, double-blind controlled trial investigates whether intraoperative intravenous methadone (0.15 mg/kg based on ideal body weight) reduces acute postoperative pain and opioid consumption in patients undergoing elective total hip arthroplasty under spinal anesthesia with mepivacaine. The primary outcome is patient-reported pain on a visual analog scale (VAS) 30-60 minutes after arrival in the post-anesthesia care unit (PACU). Secondary outcomes include opioid use, pain scores over time, incidence of nausea/vomiting, and quality of recovery. A total of 162 subjects will be enrolled at MUSC surgical sites.

Timeline

Start
2026-01-12
Primary completion
2026-12-31
Completion
2027-01-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Methadone Other / unclassified 0.15 mg/kg Intravenous

Indications

No indication recorded.