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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03967028
Other study ID # CSR
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 5, 2019
Est. completion date December 31, 2021

Study information

Verified date May 2022
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Rate of caesarean section surgery are rising worldwide,but the determinant of this increase,especially in low-income and middle-income countries, are controversial.In 1985,The world Health organization (WHO) stated;(There is no justification for any region to have a ceasearan section rate higher than 10-15%). Despite the lack of scientific evidence indicating any substantial maternal and perinatal benefits from increasing cs rates,and some studies showing that higher rates could be linked to negative consequences in maternal and child health, CS continue to increase world wide


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date December 31, 2021
Est. primary completion date September 30, 2021
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria: - Nullipara - Single fetus . - More than 37 weeks . - Patients who pass into spontaneous - Patient who induced labour Exclusion Criteria: - Non cephalic presentation. - Abnormal lie

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
cesarean section
lower segment cesarean section either elective or emergency

Locations

Country Name City State
Egypt Ahmed Abbas Assiut Cairo

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary The prevalence of etiologies of cesarean section determine the rate of cesarean section with different indication according to Robson classification one month
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