drugset / Trial / NCT04897841

Obstetric Liposomal Bupivacaine Via Surgical Transversus Abdominis Plane Block for Post Cesarean Pain Control

NCT04897841 ↗

RandomizedParallel-groupSingle-blindTreatment

Summary

This study seeks to identify whether the addition of liposomal bupivacaine to regular bupivacaine and saline administered via surgical transversus abdominis plane (TAP) block will reduce the cumulative opioid dose in the first 48 hours after cesarean. 60 women scheduled for cesarean at Unity-Point Health Meriter Hospital in Madison, Wisconsin will be enrolled and can be expect to be on study for up to 6 weeks post-partum.

Timeline

Start
2021-10-11
Primary completion
2022-08-31
Completion
2022-10-13

Outcome

Missed primary endpoint

paper compared with 8 morphine milligram equivalents (interquartile range, 0-40) among participants allocated to the control group (P=.236). PMID 38154599 ↗

Drugs

EvaluationDrugModalityDoseRoute
Background Bupivacaine Other / unclassified 20 ml Other
Background Bupivacaine Other / unclassified 0.25 % Other
Background Bupivacaine Other / unclassified 30 ml Other