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A Skin Glue Versus Subcuticular Suture for Cesarean Closure Study

NCT05903547 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 151

Last updated 2026-04-07

Study results available
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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.

Conditions

  • Cesarean Section
  • Complication
  • Wound

Interventions

DEVICE

Dermabond Prineo

For subjects in the Dermabond Prineo group, the Dermabond Prineo system will be applied to the skin for skin closure under manufacturer's guidelines.

OTHER

Suture

For subjects in the Suture group, the skin will be closed with the standard subcuticular suture method.

Sponsors & Collaborators

Principal Investigators

  • Russell Miller, MD · Columbia University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-23
Primary Completion
2024-12-06
Completion
2025-02-05
FDA Device
Yes

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05903547 on ClinicalTrials.gov