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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05900492
Other study ID # cesarean scar niche R.F
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date January 1, 2023
Est. completion date September 30, 2023

Study information

Verified date June 2023
Source Beni-Suef University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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


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


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 300
Est. completion date September 30, 2023
Est. primary completion date September 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: 1. Delivery by cesarean section. 2. More than 6 months after delivery. 3. Cesarean section by senior resident or assistant lecturer. Exclusion Criteria: 1. Single layer technique in uterine closure. 2. Uterine anomaly.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
cesarean section
caesarean delivery, is the surgical procedure by which one or more babies are delivered through an incision in the mother's abdomen

Locations

Country Name City State
Egypt Beni-suef university Hospital Bani Suwayf Beni Suef

Sponsors (1)

Lead Sponsor Collaborator
Beni-Suef University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary the incidence of cesarean scar niche among cesarean deliveries number of cases develop cesarean scar niche after cesarean deliveries 6 months after delivery
Secondary risk factors that affect the development of the niche. age- BMI- post operative infection - PROM(preterm rupture of membrane) within 1 month of delivery
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