drugset / Trial / NCT04685876

Comparing TAP Blocks Bupivacaine, and Placebo for Plane

NCT04685876

Phase 3 Completed 285 enrolled Edward Mascha
RandomizedParallel-groupTriple-blindPrevention

Summary

The study will prospectively compare the analgesic efficacy of TAP blocks with liposomal bupivacaine, plain bupivacaine, and placebo in patients who are scheduled for major abdominal surgery. The primary aim is to assess the duration of the local analgesia (determined by pinprick and cold) in all four quadrants. Comparing opioid consumption and pain scores is a secondary aim. All aims will be assessed over 72 hours or the duration of hospitalization if shorter.

Timeline

Start
2021-06-04
Primary completion
2024-02-20
Completion
2024-02-20

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bupivacaine Other / unclassified 20 ml Other
Comparator Bupivacaine Other / unclassified 50 ml Other

Indications

No indication recorded.