Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
5000 participants
OBSERVATIONAL
2019-04-30
2020-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Vaginal delivery
woman who terminate their pregnancy by vaginal delivery
vaginal delivery
pregnancy ended by vaginal delivery
Cesarean delivery
woman who terminate their pregnancy by cesarean delivery
Cesarean section
pregnancy ended by cesarean delivery
Interventions
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vaginal delivery
pregnancy ended by vaginal delivery
Cesarean section
pregnancy ended by cesarean delivery
Eligibility Criteria
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Inclusion Criteria
* Delivery between 37 and 42 weeks
* Singleton pregnancy \_ cephalic presentation
Exclusion Criteria
18 Years
40 Years
FEMALE
Yes
Sponsors
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Cairo University
OTHER
Responsible Party
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Ahmed M Maged, MD
Principal investigator
Principal Investigators
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Ahmed Maged, MD
Role: PRINCIPAL_INVESTIGATOR
Professor
Locations
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Kasr Alainy medical school
Cairo, , Egypt
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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56
Identifier Type: -
Identifier Source: org_study_id
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