NCT07075159

Hydrocolloid Dressings for Oculofacial Plastic and Reconstructive Wound Healing

• Status: Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 20 (estimated)
• Sponsor: Janice Hernandez, MD · Academic / Other
• Sex: All
• Age: 18 Years – 100 Years
• Healthy volunteers: Not accepted

Summary

This study aims to explore the use of a hydrocolloid dressing (DuoDERM EXTRA THIN) as an alternative to the current standard of care. The dressing would be applied immediately after surgery and removed at a post-operative week 1 appointment. The dressing would eliminate the need for antibiotic ointment application and reduce the burden of post-operative care on the patient.

Conditions

• Wound Healing
• Mohs Micrographic Surgery
• Oculofacial Reconstruction

Interventions

Type	Name	Description
DEVICE	Hydrocolloid Wound Dressing	one time hydrocolloid dressing application

Timeline

• Start date: 2025-02-28
• Primary completion: 2026-09-01
• Completion: 2026-09-01
• First posted: 2025-07-20
• Last updated: 2025-12-17

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study