- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04898244
Obstetricians' Views on the Reasons for Egypt's High Caesarean Section Rates
May 21, 2021 updated by: Saad El Gelany,MD, Minia University
Causes of High Caesarean Section Rates in Egypt: Perception of Obstetricians
Handling of questionnaires to a number of obstetricians from different hospitals to show their perceptions about causes of high cs rate in Egypt
Study Overview
Status
Completed
Conditions
Detailed Description
An open-ended self-administered questionnaire Handled to a number of obstetricians from different hospitals to show their perceptions about causes of the high cs rate in Egypt.
Study Type
Observational
Enrollment (Actual)
201
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Minya, Egypt
- Minia University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
28 years to 40 years (Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Obstetricians from different hospitals and areas
Description
Inclusion Criteria:
Obstetricians from different hospitals. -
Exclusion Criteria:
Refusal to participate
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Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reasons of the High Caesarean Section Rates in Egypt.
Time Frame: 12 months
|
A questionnaire filled by Obstetricians working in Egypt to explore the reasons of high Caesarean Section Rates from their point of view.
|
12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 12, 2018
Primary Completion (Actual)
August 12, 2020
Study Completion (Actual)
August 12, 2020
Study Registration Dates
First Submitted
May 15, 2021
First Submitted That Met QC Criteria
May 21, 2021
First Posted (Actual)
May 24, 2021
Study Record Updates
Last Update Posted (Actual)
May 24, 2021
Last Update Submitted That Met QC Criteria
May 21, 2021
Last Verified
May 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- MUEOB0022
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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