Status:
COMPLETED
Single Balloon Catheter Compared With Double Balloon Catheter for Ripening of the Unfavorable Cervix
Lead Sponsor:
HaEmek Medical Center, Israel
Conditions:
Induction of Labor
Eligibility:
FEMALE
18-48 years
Phase:
NA
Brief Summary
The purpose of this study is to compare between single balloon catheter and double balloon catheter for ripening the cervix among pregnant with unfavorable cervix.
Eligibility Criteria
Inclusion
- Induction of labor is indicated
- Gestational age between 24 - 42 weeks
- Singleton pregnancy
- Bishop score less than 7
Exclusion
- Any contraindication for vaginal delivery
- Previous cesarean delivery
- Low lying placenta
- Rupture of membranes
- Fetal malformations incompatible with life
- intrauterine fetal death
- Amnionitis
- Genital viral infection (HIV, hepatitis C virus
- , hepatitis B virus)
- Allergy to latex
Key Trial Info
Start Date :
June 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2010
Estimated Enrollment :
293 Patients enrolled
Trial Details
Trial ID
NCT00690040
Start Date
June 1 2008
End Date
December 1 2010
Last Update
October 24 2016
Active Locations (1)
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1
Department of Ob/Gyn, Ha'Emek Medical Center
Afula, Israel