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Completed
NCT07075159
Hydrocolloid Dressings for Oculofacial Plastic and Reconstructive Wound Healing
Conditions: Wound Healing, Mohs Micrographic Surgery, Oculofacial Reconstruction
Sex: All
Ages: 18 Years – 100 Years
Healthy volunteers: No
Phase: NA
Enrollment: 10
Sponsor: Janice Hernandez, MD
Location: University of Kentucky Lexington Kentucky
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
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 \100
* allergy to pectin, gelatin, and sodium carboxymethylcellulose
* adults with impaired consent capacity
* incarcerated individuals.
Source: ClinicalTrials.gov (NCT07075159). StuddyBuddy aggregates publicly available trial information.