Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06412978

Post-Operative Cesarean Section Cosmesis

Post-Operative Cosmesis and Skin Closure Methods After Cesarean Section

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
52 (estimated)
Sponsor
Wake Forest University Health Sciences · Academic / Other
Sex
Female
Age
18 Years – 44 Years
Healthy volunteers
Accepted

Summary

Given the high numbers of cesarean deliveries being performed today, there has been interest in optimizing surgical techniques. Several recent reviews have summarized the evidence for various steps of cesarean delivery, but surprisingly in many cases there is little scientific evidence on which to base the choice of surgical technique.

Detailed description

Cesarean delivery is the most common surgical procedure performed in the United States, with over 1 million procedures performed per year. Based on recent Center for Disease Control (CDC) National Vital Statistics Report (2021) 32.1% of all births in the United States were via cesarean delivery. Given the high numbers of cesarean deliveries being performed today, there has been interest in optimizing surgical techniques. Absorbable staples, made from a combination of polylactic and polyglycolic acid, are a relatively new option for skin closure at the time of surgery. This study is a randomized trial that will investigates two cesarean skin closure techniques-subcuticular, polyglecaprone suture (Monocryl), and absorbable subcuticular polyglycolic acid staples (INSORB)-to determine if one is associated with better scar cosmesis.

Conditions

Interventions

TypeNameDescription
PROCEDUREabsorbable subcuticular polyglycolic acid staples (INSORB)Insorb absorbable staples are used for skin closure
PROCEDUREsubcuticular, polyglecaprone suture (Monocryl)Monocryl absorbable staples are used for skin closure

Timeline

Start date
2024-09-05
Primary completion
2026-10-01
Completion
2026-10-01
First posted
2024-05-14
Last updated
2026-03-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06412978. Inclusion in this directory is not an endorsement.