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RECRUITING
NCT07227064
PHASE3

Methadone in THA for Post-op Pain and Opioid Reduction

Sponsor: Medical University of South Carolina

View on ClinicalTrials.gov

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.

Official title: Reduction of Post-op Pain and Opioid Consumption With the Addition of Methadone in Total Hip Arthroplasty: a Double-blind Randomized Control Trial

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

162

Start Date

2026-01-12

Completion Date

2027-01-31

Last Updated

2026-02-05

Healthy Volunteers

No

Interventions

DRUG

Methadone

Patients will intraoperatively receive methadone 0.15mg/kg IV, based on ideal body weight.

Locations (1)

Medical University of South Carolina

Charleston, South Carolina, United States