Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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12 December 2020 |
Main ID: |
NCT02574338 |
Date of registration:
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09/10/2015 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Cervical Ripening: A Comparison Between Intravaginal Misoprostol Tablet and Intracervical Foley's Catheter and Subsequent Induction of Labor, Safety and Efficacy in Federal Teaching Hospital Abakaliki, Ebonyi State, Nigeria.
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Scientific title:
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Date of first enrolment:
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September 2015 |
Target sample size:
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135 |
Recruitment status: |
Completed |
URL:
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https://clinicaltrials.gov/show/NCT02574338 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Double (Participant, Investigator).
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Phase:
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N/A
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Countries of recruitment
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Nigeria
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Parturients who gave consent
- has low bishop score (=5)
- term singleton cephalic presenting fetus
- intact membranes
- no contraindication to vaginal delivery
Exclusion Criteria:
- those who refused consent
- preterm delivery
- vaginal infection
- non-cephalic presentation
- multiple gestation
- low lying placenta/previa,
- vaginal bleeding,
- previous cesarean section
- rupture of membranes
Age minimum:
N/A
Age maximum:
N/A
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Cervical Ripening and Induction of Labor
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Intervention(s)
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Device: Foley's Catheter
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Drug: prostaglandin E1 analogue
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Primary Outcome(s)
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Bishop Score of 6 or more
[Time Frame: 24 hours]
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Secondary ID(s)
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MSFC-2015-CT
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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