Comparing 30mL Single Versus 80mL Double Balloon Catheters for Pre-induction Cervical Ripening
NCT ID: NCT02344459
Last Updated: 2015-01-26
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
105 participants
INTERVENTIONAL
2010-01-31
2013-11-30
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
TREATMENT
NONE
Study Groups
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80mL double balloon catheter (Cook catheter®)
mechanical pre-induction cervical ripening
The balloon catheters have been used to provide mechanical dilation to the cervix as a method of pre-induction cervical ripening.
30mL single Foley balloon catheter
mechanical pre-induction cervical ripening
The balloon catheters have been used to provide mechanical dilation to the cervix as a method of pre-induction cervical ripening.
Interventions
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mechanical pre-induction cervical ripening
The balloon catheters have been used to provide mechanical dilation to the cervix as a method of pre-induction cervical ripening.
Eligibility Criteria
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Inclusion Criteria
* Singleton
* Cephalic presentation
* Fewer than 4 contractions in 10 minutes
* Reactive fetal monitoring
Exclusion Criteria
* Placenta previa
* Vasa previa
* Unexplained vaginal bleeding
* Active herpes simplex virus infection
* Non-English speaking
* Previous attempt at an induction of labor in the current pregnancy
* Prolapsed umbilical cord
* More than one prior cesarean delivery or history of classical cesarean delivery
* Patients receiving or planning to undergo exogenous prostaglandin administration as the primary induction agent
18 Years
FEMALE
Yes
Sponsors
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University of Washington
OTHER
Responsible Party
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Kara Hoppe
Maternal Fetal Medicine Fellow
Principal Investigators
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Kara K Hoppe, DO
Role: PRINCIPAL_INVESTIGATOR
University of Washington
Other Identifiers
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36685-D
Identifier Type: -
Identifier Source: org_study_id
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