RECRUITING

Outcomes of Running Locking Suture vs Standard Running Suture 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. The most commonly performed closure technique uses running sutures, where a single strand of suture is continued along the length of the wound with a series of uninterrupted stiches. However, alternative closure techniques exist such as the running locking suture, which can offer advantages such as improved tension and thus reduce post-operative complications with better aesthetic outcome. In this study, half the wound will be stitched with standard running sutures and the other half will be stitched with running locking sutures. This will allow us to see if the side with running locking sutures heals with less scarring.

Official Title

Outcomes of Running Locking Suture vs Standard Running Suture in Surgical Wounds: a Randomized Evaluator-blinded Split-wound Comparative Effectiveness Trial

Quick Facts

Study Start:2024-08-01
Study Completion:2025-10-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06288009

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
  5. * Wounds with predicted closure length less than 3cm

Contacts and Locations

Study Contact

John Robb, BS, BA
CONTACT
9165512636
jmrobb@ucdavis.edu
Keemberly Kim, MD
CONTACT
9168161525
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 Date2024-08-01
Study Completion Date2025-10-01

Study Record Updates

Study Start Date2024-08-01
Study Completion Date2025-10-01

Terms related to this study

Keywords Provided by Researchers

  • Running Locking Suture

Additional Relevant MeSH Terms

  • Scarring