Cervical Length Pre-induction as a Tool to Predict Vaginal Birth
NCT ID: NCT02916082
Last Updated: 2016-09-27
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
200 participants
OBSERVATIONAL
2015-11-30
2016-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Prolonged pregnancy
Pregnancies with 41 weeks or more of gestation determined by a reliable last menstrual period or early fetal ultrasound.
Cervical length measurement
Vaginal ultrasound to measure cervical length previous to use of prostaglandins.
Interventions
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Cervical length measurement
Vaginal ultrasound to measure cervical length previous to use of prostaglandins.
Eligibility Criteria
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Inclusion Criteria
* Cervical length measured by a FMF certified physician
Exclusion Criteria
FEMALE
No
Sponsors
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Saint Thomas Hospital, Panama
OTHER
Responsible Party
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Osvaldo A. Reyes T.
Coordinator of Research
Locations
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Saint Thomas H
Panama City, Provincia de Panamá, Panama
Countries
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Other Identifiers
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2015-288V2
Identifier Type: -
Identifier Source: org_study_id
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