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Clinical Trials/NCT03536832
NCT03536832
Completed
Not Applicable

Comparison of Suture Materials for Subcuticular Skin Closure at Cesarean Delivery

Kanuni Sultan Suleyman Training and Research Hospital1 site in 1 country220 target enrollmentApril 15, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cesarean Section; Infection
Sponsor
Kanuni Sultan Suleyman Training and Research Hospital
Enrollment
220
Locations
1
Primary Endpoint
surgical site infection
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Subcuticular skin closure with suture after cesarean has been shown to result in lower rates of wound complications than with staple closure. However, the optimal choice of suture material for subcuticular skin closure is unclear. Vicryl vs Prolen suture materials will be used for subcuticular closure of transverse skin incisions after cesarean section. Patients will be controlled for superficial surgical site infections 1 week after the cesarean section.

Detailed Description

Cesarean section is the most common abdominal surgery worldwide. Subcuticular skin closure with suture after cesarean has been shown to result in lower rates of wound complications than with staple closure. However, the optimal choice of suture material for subcuticular skin closure is unclear. Vicryl vs Prolen suture materials will be used for subcuticular closure of transverse skin incisions after cesarean section. Patients will be controlled for superficial surgical site infections 1 week after the cesarean section.

Registry
clinicaltrials.gov
Start Date
April 15, 2018
End Date
November 1, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Berna Aslan Cetin

Md, ObGYN

Kanuni Sultan Suleyman Training and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • Age 18-40
  • women undergoing cesarean section

Exclusion Criteria

  • body mass index\>30

Outcomes

Primary Outcomes

surgical site infection

Time Frame: 1 week

infection

Study Sites (1)

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