drugset / Trial / NCT04849858

Pilot Study of Liposomal Bupivacaine Redosing in Patients Undergoing Major Gynecologic Procedures

NCT04849858

Phase 3 Terminated 13 enrolled University of California, Irvine
Non-randomizedSequentialOpen-labelTreatment

Summary

The purpose of this research study is to find out which type of transversus abdomens plane (TAP) and block (bupivacaine, liposomal bupivacaine or liposomal bupivacaine with re-dosing at 48-60 hours) improves your pain control and lowers your risk of post-operative common side effects of surgery and narcotic pain medications.

Timeline

Start
2019-05-20
Primary completion
2023-01-13
Completion
2023-01-13

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bupivacaine Other / unclassified Other