Comparing two types of stitches for surgical wounds
Outcomes of Running Locking Suture vs Standard Running Suture in Surgical Wounds: a Randomized Evaluator-blinded Split-wound Comparative Effectiveness Trial
This study is testing whether using a special type of stitch or a standard stitch after surgery on the head and neck leads to less scarring and better-looking results for patients.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of California, Davis Academic / other |
| Locations | 1 site (Sacramento, California) |
| Trial ID | NCT06288009 on ClinicalTrials.gov |
What this trial studies
This study compares the effectiveness of running locking sutures versus standard running sutures in reducing scarring after surgical procedures on the head and neck. Patients undergoing cutaneous surgery will have one side of their wound closed with standard sutures and the other side with locking sutures. The goal is to evaluate which technique results in less scarring and better aesthetic outcomes. By analyzing the healing process and post-operative complications, the study aims to provide insights into optimal wound closure methods.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older scheduled for cutaneous surgical procedures on the head or neck requiring primary closure.
Not a fit: Patients with wounds shorter than 3cm or those who are pregnant or incarcerated may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical techniques that minimize scarring for patients undergoing facial and head surgeries.
How similar studies have performed: While there have been studies on various suturing techniques, the specific comparison of running locking sutures to standard running sutures for scar reduction is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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 Exclusion Criteria: * Incarceration * Under 18 years of age * Pregnant Women * Unable to understand written and oral English * Wounds with predicted closure length less than 3cm
Where this trial is running
Sacramento, California
- University of California, Davis - Dermatology Department — Sacramento, California, United States (Recruiting)
Study contacts
- Principal investigator: Daniel Eisen, MD — University of California, Davis - Dermatology
- Study coordinator: John Robb, BS, BA
- Email: jmrobb@ucdavis.edu
- Phone: 9165512636
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.