drugset / Trial / NCT06362226
Optimizing Ocular Outcomes: A Dual-armed Study for Periorbital Burn Management
RandomizedParallel-groupOpen-labelTreatment
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.
Timeline
- Start
- 2026-06-05
- Primary completion
- 2026-06-05
- Completion
- 2026-06-05
Outcome
Outcome not reported
Stopped: “Inventory not available”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Maxitrol | Unknown | — | Topical |
| Subject | Triamcinolone | Other / unclassified | — | Subcutaneous |
| Subject | fluorouracil | Small molecule | — | Subcutaneous |