drugset / Trial / NCT06114121

Intrathecal Morphine vs. Intrathecal Morphine and Regional Anesthesia After Cesarean Section.

NCT06114121 ↗

Phase 4 Withdrawn University of Miami
RandomizedParallel-groupOpen-labelTreatment

Summary

The objective of the study is to optimize post-operative analgesia and improve patient satisfaction while reducing total opioid consumption after cesarean section

Timeline

Start
2024-07-10
Primary completion
2024-09-10
Completion
2024-09-10

Outcome

Outcome not reported

Stopped: “Study will no longer be conducted”

Drugs

EvaluationDrugModalityDoseRoute
Background Bupivacaine Other / unclassified 0.75 % —
Background Bupivacaine Other / unclassified 1.4 ml —
Background Bupivacaine Other / unclassified 1.7 ml —
Background Bupivacaine Other / unclassified 10 mg —
Background Bupivacaine Other / unclassified 12 mg —
Background Morphine Other / unclassified 100 ug Intrathecal
Background Ropivacaine Other / unclassified 0.5 % —
Background Ropivacaine Other / unclassified 20 ml —
Background Ropivacaine Other / unclassified 40 ml —

Indications

No indication recorded.