Incidence of Uterine Cesarean Scar Niche After Cesarean Delivery

Status Active, not recruiting

Clinical Trial Summary

To assess the incidence of cesarean scar niche and its risk factors in a prospectively collected population.

Clinical Trial Description

It will be carried out in Gynecology and Obstetrics department in Beni-Suef University Hospital using Ultrasound: Six months after the cesarean delivery, participants will be invited to the gynecologic outpatient clinic or department for ultrasound (US) examination to detect the presence of the niche. Women without contraception will be examined during the follicular phase of the menstrual cycle to avoid an eventual early pregnancy. Otherwise, a random phase of the menstrual cycle will be accepted. Women who are pregnant at the time of US will be excluded. Women will be examined in the lithotomy position with an empty bladder. The uterus will be examined in a standardized way, with trans-vaginal US performed first. For the diagnosis of cesarean scar niche (defined as an anechoic defect in the anterior wall of the lower uterine segment, communicating with the endometrial cavity),we will use a predetermined definition of a defect at least 2.0 mm deep ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05900492
Study type	Observational
Source	Beni-Suef University
Contact
Status	Active, not recruiting
Phase
Start date	January 1, 2023
Completion date	September 30, 2023

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See also
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