CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 232 enrolled
Drug / intervention
Randomizing to Suture or Staple closure of Cesarean sectionprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02549131
NCT02549131N/ACompleted
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Cesarean Wound Closure in Women With BMI 40 or Greater: A Randomized Controlled Trial Comparing Subcuticular Suture to Surgical Staples

Pediatrix·interventional·Posted Sep 15, 2015·Updated Aug 26, 2022

In Brief

A clinical study evaluating Randomizing to Suture or Staple closure of Cesarean section for C.Delivery; Penetration, Pregnant Uterus, by Instrument and Obesity. Completed, enrolled 232 participants across 2 sites.

Detailed Summary

The purpose of this randomized controlled prospective trial is to guide physicians on the most effective evidenced based skin closure during a cesarean section for the obese gravida, defined as a BMI of 40 or greater. The study will compare two closure methods: subcuticular sutures and surgical staples.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsC.Delivery; Penetration, Pregnant Uterus, by Instrument, Obesity
CountriesUnited States
CollaboratorsBanner Health

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedSep 15, 2015
Enrollment StartSep 1, 2015
Primary CompletionMar 1, 2020
Study CompletionJan 1, 2021
TodayJul 2, 2026
Enrollment to primary: 4.5 yearsPosted 10.8 years ago

Interventions

Randomizing to Suture or Staple closure of Cesarean sectionprocedure

Randomizing to either surgical subcuticular suture or surgical staples in women of BMI greater than 40 undergoing Cesarean section delivery.