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Subcuticular Absorbable Staples Versus Conventional Skin Closure in Women Undergoing Cesarean Delivery

Wound Heal Clinical Trial

Official title:
Subcuticular Absorbable Staples Versus Conventional Skin Closure in Women Undergoing Cesarean Delivery: A Randomized Control Trial

Clinical Trial Summary

Despite the high numbers of cesareans being performed, scientific evidence behind which surgical techniques are best remains uncertain. Our objective is to determine if subcuticular absorbable staples improve operative time and wound cosmetics.

Clinical Trial Description

This will be an open-label randomized controlled clinical trial. Women undergoing cesarean delivery will be randomized to have either standard wound closure with Monocryl suture or absorbable subcuticular staples placed by INSORB skin stapling device. The INSORB under the skin stapling device is FDA approved but not currently used as standard of care at UTMB. We will exclude women with intraamniotic infection, immunosuppression, active skin infection, those unlikely to be followed-up after delivery, or unable to provide consent. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05112640
Study type Interventional
Source The University of Texas Medical Branch, Galveston
Contact Brett Goldman, MD
Phone 9542632359
Email brgoldma@utmb.edu
Status Recruiting
Phase N/A
Start date November 16, 2021
Completion date March 31, 2024
View Details
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