Inpatient and Outpatient Balloon Catheter Cervical Ripening
NCT ID: NCT04342741
Last Updated: 2020-04-13
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
60 participants
INTERVENTIONAL
2017-08-01
2018-05-31
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
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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Foley catheter inpatient
Participants had intracervical ripening with foley catheter after admission into the ward.
Foley catheter cervical ripening
Participants were assessed when labour was established or the following morning.
Foley catheter outpatient
Participants had intracervical ripening with foley catheter and allowed home.
Foley catheter cervical ripening
Participants were assessed when labour was established or the following morning.
Interventions
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Foley catheter cervical ripening
Participants were assessed when labour was established or the following morning.
Eligibility Criteria
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Inclusion Criteria
* gestational age beyond 37 weeks
* cephalic presentation
* intact membranes
* Bishop score less than 6
* lives within 10km from National University Malaysia Medical Centre or able to reach within 30 minutes
* readily available transport
Exclusion Criteria
* intrauterine fetal growth restriction
* estimated fetal weight more than 4000gram
* fetal anomalies
* abnormal pre-induction cardiotocograph
* non-vertex presentation
* unstable lie
* sepsis
* hypertension
* allergy to latex
* previous uterine scar
* history of antepartum haemorrhage
* parity of 6 and more
* placenta praevia
* suspected cephalopelvic disproportion
18 Years
FEMALE
Yes
Sponsors
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National University of Malaysia
OTHER
Responsible Party
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Rahana Abd Rahman
Co-primary investigator
Locations
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UKM Medical Centre
Cheras, Kuala Lumpur, Malaysia
Countries
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Other Identifiers
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FF-2017-358
Identifier Type: -
Identifier Source: org_study_id
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