A Skin Glue Versus Subcuticular Suture for Cesarean Closure Study

Completed · Not applicable

Conditions studied: Cesarean Section, Complication, Wound

In brief

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.

Key facts

Study ID

NCT05903547

Run by

Columbia University

People needed

151

Starts

2023-08-23

Expected to finish

2025-02-05

Last updated by the study team

2026-04-07

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women age 18 years or older
• All women scheduled for primary or repeat cesarean deliveries
• All women undergoing intrapartum or antepartum cesarean delivery
• Pfannenstiel skin incision
• Birth of a live infant at time of cesarean delivery

You may not qualify if…

• Vertical skin incision
• Cesarean hysterectomy
• Emergency or stat cesarean delivery excluding standard preoperative preparation measures (i.e., use of Chlorhexidine skin prep, vaginal prep, etc)
• Intrapartum stillbirth
• Planned postpartum follow up at another facility
• Contraindications to routine postpartum pain medications
• Adhesive or tape allergy

Where it is running

• Columbia University Irving Medical Center/NYP — New York, New York, United States

Full record on ClinicalTrials.gov

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