Hydrocolloid Dressings for Oculofacial Plastic and Reconstructive Wound Healing
Recruiting
N/A
Interventional Study
Wound Healing
Mohs Micrographic Surgery
Oculofacial Reconstruction
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 100
- Sex
- Any
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 20 (estimated)
- Sponsor
- Janice Hernandez, MD · Other
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About This Trial
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.
Trial Locations
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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 \<18 years of age …
Contacts