RECRUITING

Hydrocolloid Dressings for Oculofacial Plastic and Reconstructive Wound Healing

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Hydrocolloid Dressings for Oculofacial Plastic and Reconstructive Wound Healing

Quick Facts

Study Start:2025-07-20
Study Completion:2026-03-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07075159

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 100 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients \>18 years of age
  2. * follow-up at specified intervals (1 week/6 week/3 months) in an office setting
  3. * can give informed consent
  4. * no patients will be excluded on the basis of gender, ethnicity, or religious background
  1. * Patients \<18 years of age or \>100
  2. * allergy to pectin, gelatin, and sodium carboxymethylcellulose
  3. * adults with impaired consent capacity
  4. * incarcerated individuals.

Contacts and Locations

Study Contact

Connie Dampier
CONTACT
859-562-0750
dampier@uky.edu

Principal Investigator

Janice Hernandez, MD
PRINCIPAL_INVESTIGATOR
University of Kentucky

Study Locations (Sites)

University of Kentucky
Lexington, Kentucky, 40508
United States

Collaborators and Investigators

Sponsor: Janice Hernandez, MD

  • Janice Hernandez, MD, PRINCIPAL_INVESTIGATOR, University of Kentucky

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-07-20
Study Completion Date2026-03-01

Study Record Updates

Study Start Date2025-07-20
Study Completion Date2026-03-01

Terms related to this study

Additional Relevant MeSH Terms

  • Wound Healing
  • Mohs Micrographic Surgery
  • Oculofacial Reconstruction