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NCT03173482 Clinical Trial

Prevalence of Cesarean Section on Demand in Assiut University Hospital & Abnob Central Hospital

Cesarean Section Clinical Trial

Official title:
Prevalence of Cesarean Section on Demand in Assiut University Hospital & Abnob Central Hospital

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03173482
Other study ID # CSD
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 1, 2017
Est. completion date August 31, 2018

Study information
Verified date August 2021
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Cesarean section on demand: defined as a primary cesarean section performed at the mother's request to avoid a vaginal birth, without any recognized medical or obstetric indication. The medical field now acknowledges a patient's right to actively participate in her choice of medical treatments, including method of delivery. There are many reasons for a cesarean section on demand: fear of delivery, fear of pain, family pressure, a previous bad experience, more control over events, improved care, and maintaining the integrity of the pelvic floor. of the pelvic floor.

Recruitment information / eligibility
Status Completed
Enrollment 144
Est. completion date August 31, 2018
Est. primary completion date June 30, 2018
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria: - Accepting to participate in the study. - pregnant Women undergoing Cesarean section Exclusion Criteria: - pregnant Women undergoing Cesarean section due to medical or obstetric indication - Caesarean hysterectomy .

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• questionnaire
asking about details of indication of cesarean section

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 percentage of cesarean section on request in patients through a questionnaire 1 year
See also
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Terminated NCT03695172 - Comparison of TAP, Anterior QL, or ESP Block for Elective Cesarean Section Phase 4
Recruiting NCT06247852 - Persistent Pain After Cesarean Delivery - A Danish Multicenter Cohort Study
Completed NCT06012747 - Pain After Cesarean Section - A Danish Multicenter Cohort Study.
Not yet recruiting NCT05187520 - Naldebain for Control of Post-Cesarean Section Pain Phase 2
Not yet recruiting NCT04999670 - Fascial Closure and Post-caesarean Pain N/A