Hydrocolloid Dressings for Oculofacial Plastic and Reconstructive Wound Healing

Recruiting now · Not applicable

Conditions studied: Wound Healing, Mohs Micrographic Surgery, Oculofacial Reconstruction

In brief

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.

Key facts

Study ID

NCT07075159

Run by

Janice Hernandez, MD

People needed

20

Starts

2025-02-28

Expected to finish

2026-09-01

Last updated by the study team

2025-12-17

Who can join

Age: 18 and older, up to 100. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients >18 years of age
• follow-up at specified intervals (1 week/6 week/3 months) in an office setting
• can give informed consent
• no patients will be excluded on the basis of gender, ethnicity, or religious background

You may not qualify if…

• Patients <18 years of age or >100
• allergy to pectin, gelatin, and sodium carboxymethylcellulose
• adults with impaired consent capacity
• incarcerated individuals.

Where it is running

• University of Kentucky — Lexington, Kentucky, United States (enrolling)

Full record on ClinicalTrials.gov

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