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Trial Comparing Barbed and Non-barbed Suture for Uterine Incision Closure at Cesarean Section — barbed  

Cesarean Section Clinical Trial

Official title:
Randomized Trial Comparing Barbed and Non-barbed Suture for Uterine Incision Closure at Cesarean Section

Clinical Trial Summary

This was an unblinded randomized controlled trial. Women were randomized to uterine closure with the knotless barbed suture (Stratafix PDS, Ethicon) or Vicryl (Ethicon) at the time of elective cesarean. The primary outcome was closure time of the uterine incision. Also measured were blood loss during incision closure and the use of additional hemostatic sutures. Informed consent was obtained

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02962011
Study type Interventional
Source Ziv Hospital
Contact
Status Completed
Phase Phase 3
Start date August 1, 2016
Completion date August 2017
View Details
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