Back to Trials
NCT07075159NARecruiting

Hydrocolloid Dressings for Oculofacial Plastic and Reconstructive Wound Healing

Janice Hernandez, MD

Start Date

2/28/2025

Completion Date

9/1/2026

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.

Eligibility Criteria

Age Range: 18 years to 100 years

Inclusion Criteria: * 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 Exclusion Criteria: * Patients \<18 years of age or \>100 * allergy to pectin, gelatin, and sodium carboxymethylcellulose * adults with impaired consent capacity * incarcerated individuals.

Interventions

DEVICE

Hydrocolloid Wound Dressing

Interested in This Trial?

Contact the trial locations directly using the information below to learn more about enrollment.

Expressing interest lets you review the study and consent before we connect you with the research site.

Conditions

Wound HealingMohs Micrographic SurgeryOculofacial Reconstruction

Locations

University of Kentucky

Lexington, Kentucky 40508

United States