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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COMPLETED
NA
600 participants
INTERVENTIONAL
2018-04-01
2018-11-10
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
PREVENTION
NONE
Study Groups
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Cord drainage
Cord drainage
Cord drainage
Cord clamping
Cord clamping
Cord clamping
Interventions
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Cord drainage
Cord drainage
Cord clamping
Cord clamping
Eligibility Criteria
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Inclusion Criteria
* Pregnancy with vertex presentation.
* Gestational age37 up to 42 weeks
* Patient expected to have spontaneous vaginal delivery.
* Maternal age 18 years old or more.
Exclusion Criteria
* Antepartum hemorrhage
* Multiple pregnancies
* Instrumental deliveries
* Coagulation disorders
* Over distended uterus (hydramnios, large fetus).
* Patient with extensive extended vaginal or cervical tear.
* Rupture uterus.
* Secondary arrest of cervical dilatation.
* Persistent occipito-posterior.
* Deep transverse arrest of fetal head.
18 Years
40 Years
FEMALE
No
Sponsors
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Ain Shams University
OTHER
Responsible Party
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Mohamed S Sweed, MD
Principal Investigator
Locations
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Ain Shams University Maternity Hospital
Cairo, , Egypt
Countries
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Other Identifiers
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AS1751
Identifier Type: -
Identifier Source: org_study_id
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