Amniotic Membrane for Donor Site Healing
Completed · Not applicable
Conditions studied: Burns
In brief
The purpose of this study is to compare the effectiveness of applying amniotic membrane dressings compared to gentamicin and xeroform dressings to donor sites for skin grafts. This study will enroll ten participants who undergoing a split thickness skin graft procedure with two or more donor sites. The amniotic membrane will be applied to one donor site and a dressing of xeroform and gentamicin will be applied to another other donor site. Each participant will receive both types of dressing and will serve as their own control. Postoperative follow up will follow standard of care, regardless of the dressing type. Dressings will be removed on postoperative day 4 and participants will return to be re-examined one week after being discharged from the hospital.
Key facts
- Study ID
- NCT02947737
- Run by
- Emory University
- People needed
- 4
- Starts
- 2017-02-01
- Expected to finish
- 2017-08-31
- Last updated by the study team
- 2018-05-21
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- undergoing a split thickness skin graft procedure with two or more donor sites
You may not qualify if…
- less than 18 years of age
Where it is running
- Grady Health System — Atlanta, Georgia, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.