Status:
COMPLETED
A Randomized, Control Trial for Preinduction Cervical Ripening
Lead Sponsor:
The University of Texas Health Science Center, Houston
Conditions:
Labor, Induced
Eligibility:
FEMALE
Phase:
PHASE2
Brief Summary
The goal of this study is to compare the vaginal delivery rates in women undergoing induction of labor with an unripe cervix between oxytocin induction alone and preinduction cervical ripening with pr...
Eligibility Criteria
Inclusion
- Women that are hospitalized for induction of labor that have a Bishop's score \<5
- singleton gestation
- cephalic presentation
- 24 weeks gestational age
Exclusion
- Prior uterine surgery
- malpresentation
- placenta previa or abruption
- clinically suspected or diagnosed intra amniotic infection
- genital HSV infection
- multiple gestation
- premature rupture of the membranes
- active labor
- maternal/fetal conditions that may preclude labor induction in the opinion of the investigators
Key Trial Info
Start Date :
January 1 2004
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 1 2007
Estimated Enrollment :
540 Patients enrolled
Trial Details
Trial ID
NCT00393731
Start Date
January 1 2004
End Date
August 1 2007
Last Update
January 16 2008
Active Locations (1)
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1
Lyndon B. Johnson Hospital
Houston, Texas, United States, 77026