Overview

Optimizing Ocular Outcomes: A Dual-armed Study for Periorbital Burn Management

Status:
NOT_YET_RECRUITING
Trial end date:
2027-01-01
Target enrollment:
Participant gender:
Summary
The purpose of this study is to evaluate the effectiveness in using subcutaneous 5-FU/Kenalog \& topical Maxitrol Ophthalmic ointment as different therapeutic adjuncts in the prevention of pathologic remodeling after periorbital burns.
Phase:
PHASE1
Details
Lead Sponsor:
Virginia Commonwealth University
Treatments:
Anti-Bacterial Agents
Maxitrol
Steroids