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Clinical Trial Summary

The purpose of this study is to evaluate the effectiveness in using subcutaneous 5-FU/Kenalog & antibiotic ointment with vitamin E as different therapeutic adjuncts in the prevention of pathologic remodeling after periorbital burns.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06362226
Study type Interventional
Source Virginia Commonwealth University
Contact Nikisha Richards, MD, FACS
Phone 804-828-8643
Email nikisha.richards@vcuhealth.org
Status Not yet recruiting
Phase N/A
Start date June 2024
Completion date October 2026