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
NA
100 participants
INTERVENTIONAL
2015-06-30
2016-02-29
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SCREENING
SINGLE
Study Groups
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group A
natural cesarean section
natural cesarean section
group B
traditional cesarean section
traditional cesarean section
Interventions
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natural cesarean section
traditional cesarean section
Eligibility Criteria
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Inclusion Criteria
2. full term
3. cephalic
4. single baby
5. average weight
6. spinal anathesia
Exclusion Criteria
2. Women with known or suspected fetal malformation.
3. Women with uterine malformations.
4. Breech or transverse lie.
5. Emergency caesarean section.
6. Previous two or more caesarean section
20 Years
40 Years
FEMALE
Yes
Sponsors
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Ain Shams University
OTHER
Responsible Party
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Samer mohamed ahmed
obstetric and gynecology resident
Other Identifiers
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Nsc_123
Identifier Type: -
Identifier Source: org_study_id
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