This study is currently not recruiting participants.

A Prospective Analysis Describing the Innovative Use of Liposomal Bupivacaine to Manage Donor Site Pain in Burn Patients

Study on Postoperative Anesthesia for Skin Graft Donor Sites

Not Recruiting
100 years or below
All
Phase N/A
1 Location

Brief description of study.

The purpose of this study is to evaluate the efficacy, safety, magnitude, and duration of postoperative anesthesia with liposomal bupivacaine versus traditional pain management strategies of skin graft donor sites in burn or plastics patients.

Detailed description of study

The purpose of this study is to evaluate the efficacy, safety, magnitude, and duration of postoperative anesthesia with liposomal bupivacaine versus traditional pain management strategies of skin graft donor sites in burn or plastics patients.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: burn
  • Age: 100 years or below
  • Gender: All

This study investigates the effectiveness and safety of postoperative anesthesia using an investigational medication compared to traditional pain management methods for patients who have undergone skin grafts due to burns or plastic surgery. The investigational medication is designed to provide prolonged pain relief after surgery.

Participants in the study will receive either the investigational medication or traditional pain management. The study will measure how well each method controls pain and the duration of pain relief provided. This will help determine the best approach for managing postoperative pain in skin graft donor sites.

  • Who can participate: Eligibility criteria will be determined by the research team.
  • Study details: Participants will be randomly assigned to receive either the investigational medication or traditional pain management. The investigational medication is a type of anesthesia that is expected to last longer than standard treatments.
Updated on 19 Feb 2024. Study ID: 1607705792

Interested in the study?

Select a study center that’s convenient for you, and get in touch with the study team.

Connect with the study team