Liposomal Bupivacaine Versus Lidocaine for Skin Graft Donor Site Pain

Description

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.

Conditions

Pain, Postoperative, Burns

Study Overview

Study Details

Study overview

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.

Prospective Study of Liposomal Bupivacaine for Pain Control of Split Thickness Skin Graft Donor Sites

Liposomal Bupivacaine Versus Lidocaine for Skin Graft Donor Site Pain

Condition
Pain, Postoperative
Intervention / Treatment

-

Contacts and Locations

Kansas City

The University of Kansas Health System, Kansas City, Kansas, United States, 66160

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Spanish/English speaking
  • * \<20%TBSA; \<5% TBSA deep partial or full thickness burns
  • * chronic pain syndrome
  • * \> 20% TBSA burn injury; \> 5% TBSA deep partial or full thickness burn
  • * pregnant
  • * allergy to lidocaine or other local anesthetics
  • * burns to anterior thighs

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Kansas Medical Center,

Study Record Dates

2025-12-31