Skin Glue Cesarean Study

Status Recruiting

Clinical Trial Summary

The aim of this study is to compare cesarean incision outcomes between patients with incision closed with the Dermabond Prineo system compared to standard subcuticular suture.

Clinical Trial Description

The purpose of this study is to assess patient satisfaction with their incision after undergoing cesarean delivery. Patient satisfaction with their cesarean scar at 4-6 weeks after their surgery will be compared amongst women receiving skin closure with the Dermabond Prineo skin adhesive system versus standard subcuticular suture. Dermabond Prineo has been shown to have improved cosmesis outcomes in non-obstetric populations but has not yet been studied for women receiving cesarean section. In addition to scar appearance, outcomes such as wound infection, postoperative pain, and operative time will be assessed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05903547
Study type	Interventional
Source	Columbia University
Contact	Kristine Brown, MD
Phone	919-636-1735
Email	kb3226@cumc.columbia.edu
Status	Recruiting
Phase	N/A
Start date	August 23, 2023
Completion date	April 2024

View Details

See also
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