Actively Recruiting
Hydrocolloid Dressings for Oculofacial Plastic and Reconstructive Wound Healing
Led by Janice Hernandez, MD · Updated on 2025-12-17
20
Participants Needed
1
Research Sites
78 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
Official Title
Hydrocolloid Dressings for Oculofacial Plastic and Reconstructive Wound Healing
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients over 18 years of age
- Willing to follow up at 1 week, 6 weeks, and 3 months in an office setting
- Able to give informed consent
- No exclusion based on gender, ethnicity, or religious background
You will not qualify if you...
- Patients younger than 18 years or older than 100 years
- Allergy to pectin, gelatin, or sodium carboxymethylcellulose
- Adults with impaired consent capacity
- Currently incarcerated individuals
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Kentucky
Lexington, Kentucky, United States, 40508
Actively Recruiting
Research Team
C
Connie Dampier
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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