RECRUITING

Liposomal Bupivacaine Versus Lidocaine for Skin Graft Donor Site Pain

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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.

Official Title

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

Quick Facts

Study Start:2019-03-18
Study Completion:2025-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03854344

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.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Spanish/English speaking
  2. * \<20%TBSA; \<5% TBSA deep partial or full thickness burns
  1. * chronic pain syndrome
  2. * \> 20% TBSA burn injury; \> 5% TBSA deep partial or full thickness burn
  3. * pregnant
  4. * allergy to lidocaine or other local anesthetics
  5. * burns to anterior thighs

Contacts and Locations

Study Contact

Jessica Reynolds, BSN
CONTACT
913-588-0044
jreynolds11@kumc.edu
Dhaval Bhavsar, MD
CONTACT
913-588-2000
dbhavsar@kumc.edu

Study Locations (Sites)

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

Collaborators and Investigators

Sponsor: University of Kansas Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2019-03-18
Study Completion Date2025-12-31

Study Record Updates

Study Start Date2019-03-18
Study Completion Date2025-12-31

Terms related to this study

Additional Relevant MeSH Terms

  • Pain, Postoperative
  • Burns