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Hydrocolloid Dressings for Oculofacial Plastic and Reconstructive Wound Healing

Hydrocolloid Dressings for Oculofacial Plastic and Reconstructive Wound Healing

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07075159
Acronym
HCD Wound Heal
Enrollment
10
Registered
2025-07-20
Start date
2025-02-28
Completion date
2026-02-18
Last updated
2026-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mohs Micrographic Surgery, Oculofacial Reconstruction, Wound Healing

Brief 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.

Interventions

DEVICEHydrocolloid Wound Dressing

one time hydrocolloid dressing application

Sponsors

Janice Hernandez, MD
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Number of participants with wound dehiscence3 monthsYES/NO type question if wound dehiscence is present after removal of the patch

Secondary

MeasureTime frameDescription
Patient and Observer Scar Assessment Scale3 monthsPatient and Observer Scar Assessment Scale filled out by both patient and provider at postoperative visit of both HCD Dressing and ointment. This survey is scaled from 0-10, with 0 being normal skin and 10 being very different skin. Lower scores are desired on this survey.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORJanice Hernandez, MD

University of Kentucky

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 18, 2026