RecruitingNot ApplicableNCT07075159
Hydrocolloid Dressings for Oculofacial Plastic and Reconstructive Wound Healing
Sponsor
Janice Hernandez, MD
Enrollment
20 participants
Start Date
Feb 28, 2025
Study Type
INTERVENTIONAL
Conditions
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
Min Age: 18 YearsMax Age: 100 Years
Inclusion Criteria4
- 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 Criteria4
- Patients <18 years of age or >100
- allergy to pectin, gelatin, and sodium carboxymethylcellulose
- adults with impaired consent capacity
- incarcerated individuals.
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Interventions
DEVICEHydrocolloid Wound Dressing
one time hydrocolloid dressing application
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07075159
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