Actively Recruiting
Outcomes of Running Locking Suture vs Standard Running Suture in Surgical Wounds
Led by University of California, Davis · Updated on 2025-12-05
50
Participants Needed
1
Research Sites
113 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Outcomes of Running Locking Suture vs Standard Running Suture in Surgical Wounds
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years of age or older
- Able to give informed consent themselves
- Patient scheduled for cutaneous surgical procedure on the head or neck with predicted primary closure
- Willing to return for follow up visit
You will not qualify if you...
- Incarceration
- Under 18 years of age
- Pregnant Women
- Unable to understand written and oral English
- Wounds with predicted closure length less than 3cm
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University of California, Davis - Dermatology Department
Sacramento, California, United States, 95816
Actively Recruiting
Research Team
J
John Robb, BS, BA
CONTACT
K
Keemberly Kim, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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