Clinical Trials Directory

Trials / Completed

CompletedNCT03120806

Interrupted Versus Continuous Subcuticular Skin Suturing in Elective Cesarean Section.

Comparative Study Between Interrupted and Continuous Subcuticular Skin Suturing in Women Undergoing Elective Cesarean Section. A Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
169 (actual)
Sponsor
Cairo University · Academic / Other
Sex
Female
Age
19 Years – 39 Years
Healthy volunteers
Not accepted

Summary

Non-diabetic pregnant women who undergo elective CS will be randomized into two groups: group I included women who has their skin closed with subcuticular interrupted mattress suture using non-absorbable polypropylene, and group II included women who has their skin closed with subcuticular continous suture using the same suture material

Detailed description

Non-diabetic pregnant women who undergo elective CS will be randomized into two groups: group I included women who had their skin closed with subcuticular interrupted mattress suture using non-absorbable polypropylene, and group II included women who had their skin closed with subcuticular continous suture using the same suture material.

Conditions

Interventions

TypeNameDescription
PROCEDUREInterrupted subcuticular skin closureskin is closed with interrupted mattress subcuticular sutures using non-absorbable polypropylene after elective cesarean section
PROCEDUREcontinuous subcuticular skin closureskin is closed with continuous subcuticular sutures using non-absorbable polypropylene after elective cesarean section

Timeline

Start date
2017-04-16
Primary completion
2017-12-01
Completion
2017-12-20
First posted
2017-04-19
Last updated
2021-12-23

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03120806. Inclusion in this directory is not an endorsement.