drugset / Trial / NCT03353363

Wound Infiltration of Liposomal Bupivacaine v Plain Bupivacaine for Post-Op Pain Control in Elective Cesarean Delivery

NCT03353363 ↗

Phase 4 Unknown 132 enrolled Brooke Army Medical Center
RandomizedParallel-groupTriple-blindTreatment

Summary

Randomized double blind placebo controlled trial to compare the post-operative pain control advantages of post-incisional wound infiltration with liposomal bupivacaine to plain bupivacaine in patients presenting for elective caesarean delivery.

Timeline

Start
2017-10-18
Primary completion
2018-10-18
Completion
2019-02-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Bupivacaine Other / unclassified 100 mg Other
Subject Bupivacaine Other / unclassified 266 mg Other

Indications

No indication recorded.