RECRUITING

Aesthetic Outcome of Tie-over Bolster Application in Surgical Wounds

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

When patients have surgery on the head and face, stitches are the standard way to close the wound. Wounds always result in a scar, but doctors are always looking for ways to reduce scarring. Several studies have been done to test ways to close wounds that reduce scarring. One idea is to reduce the tension around the cut. One way to reduce tension is to stitch a small piece of a special gauze over the top of the regular stitches. This procedure is called a "tie-over bolster dressing." As the name implies, this extra dressing "bolsters" the wound closure so that the skin on each side of the cut stays in place. The bolster dressing procedure has been used in the past in special cases, such as when skin grafts are necessary. The bolster dressing helps the skin graft heal by making sure the graft stays exactly in place. Keeping the wound stable with a bolster dressing also reduces bleeding under the wound. For non-grafted wounds, the bolster dressing procedure has not normally been used, and has not been well-studied. In this study the whole wound will be stitched normally and then the bolster dressing will be applied over half of the wound. This will allow us to see if the side with the bolster dressing heals with less scarring.

Official Title

Aesthetic Outcome of Tie-over Bolster Application in Surgical Wounds: a Randomized Evaluator-blinded Split-wound Comparative Effectiveness Trial.

Quick Facts

Study Start:2023-10-10
Study Completion:2025-03-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05758168

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 18 years of age or older
  2. * Able to give informed consent themselves
  3. * Patient scheduled for cutaneous surgical procedure on the head or neck with predicted primary closure
  4. * Willing to return for follow-up visit
  1. * Incarceration
  2. * Under 18 years of age
  3. * Pregnant women
  4. * Unable to understand written and oral English Wounds with predicted closure length less than 3cm

Contacts and Locations

Study Contact

John Robb, BS
CONTACT
916-551-2636
jmrobb@ucdavis.edu
Keemberly Kim, MD
CONTACT
916-816-1525
keekim@ucdavis.edu

Principal Investigator

Daniel Eisen, MD
PRINCIPAL_INVESTIGATOR
University of California, Davis - Dermatology

Study Locations (Sites)

University of California, Davis - Dermatology Department
Sacramento, California, 95816
United States

Collaborators and Investigators

Sponsor: University of California, Davis

  • Daniel Eisen, MD, PRINCIPAL_INVESTIGATOR, University of California, Davis - Dermatology

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 Date2023-10-10
Study Completion Date2025-03-31

Study Record Updates

Study Start Date2023-10-10
Study Completion Date2025-03-31

Terms related to this study

Keywords Provided by Researchers

  • Tie-over Bolster

Additional Relevant MeSH Terms

  • Scarring