drugset / Trial / NCT06826742

Intravenous Methadone Versus Intrathecal Morphine for Analgesia Following Cesarean Delivery

NCT06826742

Phase 4 Completed 30 enrolled Mayo Clinic
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to determine if there is a difference in opioid requirements at 0-48 hours after scheduled cesarean delivery in patients receiving 150 mcg intrathecal morphine compared to 0.2 mg/kg (maximum 20 mg) intravenous methadone.

Timeline

Start
2025-02-12
Primary completion
2025-09-14
Completion
2025-09-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Methadone Other / unclassified 0.2 mg/kg Intravenous
Comparator Morphine Other / unclassified 150 ug Intrathecal

Indications

No indication recorded.