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NCT04076904 Clinical Trial

Cesarean Niche Examination by Transvaginal us

Cesarean Section; Dehiscence Clinical Trial

Official title:
Cesarean Niche Examination by us to Assess Its Integrity and Dehescence

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04076904
Other study ID # cesarean niche
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 1, 2019
Est. completion date January 28, 2020

Study information
Verified date May 2020
Source Aljazeera Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The developed uterine scar developing due to cesarean section is usually clinically evaluated and visualized by transvaginal sonography (TVS) and saline infusion sonography (SIS) or Gel installation sonography (GIS)

Description:

In 2015, WHO displayed and reveled a systematic review of the research studies in the scientific literature to evaluate and asses the linkage and connection between cesarean section rates and maternal

Recruitment information / eligibility
Status Completed
Enrollment 110
Est. completion date January 28, 2020
Est. primary completion date January 25, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 42 Years
Eligibility Inclusion Criteria:

- women with secondary infertility

Exclusion Criteria:

- obstructed labor, pregnant women having chronic diseases;

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• transvaginal us with 2D and 3D SHG
transvaginal us is made to all women with SHG

Locations
Country Name City State
Egypt Algazeerah Giza
Egypt Algazeerah and Kasralainy hospital Giza

Sponsors (1)
Lead Sponsor Collaborator
Aljazeera Hospital

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary The number of women who will have dehesent scar transvaginal us showing lower segment with assessing scar within a week
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