drugset / Trial / NCT03854344

Liposomal Bupivacaine Versus Lidocaine for Skin Graft Donor Site Pain

NCT03854344 ↗

Phase 4 Completed 74 enrolled University of Kansas Medical Center
RandomizedSingle-groupSingle-blindTreatment

Summary

Donor site pain study comparing post-operative donor site pain and opioid consumption after use of Lidocaine, Liposomal Bupivicaine or regional nerve block for split thickness skin graft harvesting in patients with less than 20% TBSA burn wounds and less than %5 Deep partial or full thickness burn wounds.

Timeline

Start
2019-03-18
Primary completion
2025-08-06
Completion
2025-10-27

Outcome

Missed primary endpoint

paper There were no statistical differences in pain scores at any time point postoperatively PMID 34216466 ↗

paper There were no statistical differences in opioid consumption at 24, 48, or 72 h postoperatively between the groups PMID 34216466 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Bupivacaine Other / unclassified 266 mg Subcutaneous
Subject Bupivacaine Other / unclassified — —
Comparator Lidocaine Other / unclassified 50 mg Subcutaneous

Indications