Actively Recruiting
Comparing Two Skin Closure Methods for Cesarean Section to Improve Scar Appearance
Led by Wake Forest University Health Sciences · Updated on 2026-03-16
52
Participants Needed
1
Research Sites
N/A
Total Duration
AI-Summary
What this Trial Is About
Cesarean delivery is the most common surgical procedure in the United States, with over 1 million procedures annually. Around 32.1% of all births occur via cesarean delivery, creating interest in optimizing surgical techniques. This trial evaluates two skin closure methods after cesarean section to determine which results in better scar appearance and cosmesis. The study compares absorbable subcuticular polyglycolic acid staples INSORB and subcuticular polyglecaprone sutures Monocryl for closing the skin after cesarean delivery. Participants will be randomly assigned to receive one of these two skin closure techniques during their scheduled cesarean section. Both methods use absorbable materials designed to close the skin effectively. Participants will be monitored for six weeks after surgery. Researchers will assess scar cosmetic scores along with wound complications, hospital stay length, and use of pain medications such as intravenous opiates and oral NSAIDs. Patient-reported pain and satisfaction with scar appearance will also be collected. This follow-up period allows evaluation of healing and patient experience related to the closure method used.
CONDITIONS
Brief Title
Post-Operative Cesarean Section Cosmesis
Research Team
C
Christina Tulbert
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
