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Clinical Trial Summary

The aim of this randomized control trial is to compare the residual myometrial thickness and the depth of cesarean section scar defect after uterine incision closure with barbed or conventional sutures.


Clinical Trial Description

The aim of this randomized control trial is to compare the residual myometrial thickness and the depth of cesarean section scar defect after uterine incision closure with barbed or conventional sutures. Primigravida patients undergoing transverse lower segment cesarean section will be included in the study.Cesarean section incision will be closed with double layers of continuous barbed or conventional sutures. Ultrasound examination will be performed 6 months after the operation to measure the residual myometrial thickness and the scar depth. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03182010
Study type Interventional
Source Cairo University
Contact Usama M Fouda, Prof.
Phone 01095401375
Email umfrfouda@yahoo.com
Status Not yet recruiting
Phase N/A
Start date August 2017
Completion date August 2020

See also
  Status Clinical Trial Phase
Recruiting NCT02865655 - Cesarean Section Scar Evaluation by Saline Contrast Sonohysterography During Hysteroscopy N/A