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The aim of this study is to compare the effectiveness and safety of Foley's catheter and misoprostol in cervical ripening.
This is a randomized clinical study which will be made up of two arms or groups. The first arm or group - 1 will have cervical ripening with intracervical extraamniotic Foley's catheter while group - 2 will have cervical ripening with intravaginal misoprostol. The parturients will be randomly selected by simple lottery and recruited into the two arms of the study. Each parturient will pick by simple lucky dip from a pool of folded papers with inscription group 1 or group 2 in a bag in a double blinded manner and will be recruited into the group picked among the two arms of the study. The Bishop's score of the cervix will be accurately determined and documented before cervical ripening. Bishop's score of ≥6 will be considered ripe. Oxytocin will be used for induction or augmentation of labor as required.
Age
All ages
Sex
FEMALE
Healthy Volunteers
Yes
Federal Teaching Hospital, Abakaliki
Abakaliki, Ebonyi State, Nigeria
Start Date
September 1, 2015
Primary Completion Date
August 1, 2018
Completion Date
August 1, 2018
Last Updated
October 15, 2019
135
ACTUAL participants
Foley's Catheter
DEVICE
prostaglandin E1 analogue
DRUG
Lead Sponsor
Nwali Matthew Igwe
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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