drugset / Trial / NCT05069012

Intrathecal Morphine for Cesarean Delivery

NCT05069012 ↗

Phase 4 Completed 72 enrolled Beth Israel Deaconess Medical Center
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomized double blinded non-inferiority study comparing the duration of pain relief when patients receive one of three doses of spinal morphine. Enrolled patients will be randomly assigned to receive either 50 mcg, 150 mcg, or 250 mcg. All patients will receive standardized postoperative care, including multimodal analgesia. The primary outcome will be the time until the patient requests additional opioid pain medications.

Timeline

Start
2021-11-15
Primary completion
2022-07-23
Completion
2022-07-23

Drugs

EvaluationDrugModalityDoseRoute
Comparator Morphine Other / unclassified 50 ug Intrathecal
Comparator Morphine Other / unclassified 150 ug Intrathecal
Comparator Morphine Other / unclassified 250 ug Intrathecal

Indications

No indication recorded.