Status:
COMPLETED
The Comparison of Efficacy for Cervical Ripening in Labor Induction Between Titrated and Conventional Oral Misoprostol
Lead Sponsor:
Mahidol University
Conditions:
Cervical Ripening
Labor Induction
Eligibility:
FEMALE
18-45 years
Phase:
PHASE4
Brief Summary
The purpose of this study is to compare the efficacy for cervical ripening in labor induction between titrated and conventional oral misoprostol
Eligibility Criteria
Inclusion
- age 18 years old or more
- singleton pregnancy at 37 weeks gestation or more
- cephalic presentation
- reassuring fetal heart rate pattern
- admission for labor induction due to medical or obstetrical conditions
- bishop score less than 6
- giving consent and having signed the consent form for this study
Exclusion
- parity more than 3
- estimated fetal weight more than 3,500 grams
- non-reassuring fetal heart rate pattern
- having contraindication for vaginal delivery
- previous uterine scar
- suspected abruptio placenta with non-reassuring fetal heart rate pattern
- abnormal bleeding per vagina, except bloody show
- PROM
- having underlying cardiac, hepatic, or renal diseases
- having history of allergy to misoprostol or prostaglandin analogues
- cervical dilatation 3 centimeters or more
- uterine contraction 3 times or more in 10 minute
Key Trial Info
Start Date :
May 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2010
Estimated Enrollment :
64 Patients enrolled
Trial Details
Trial ID
NCT00886860
Start Date
May 1 2009
End Date
March 1 2010
Last Update
July 14 2010
Active Locations (1)
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1
Siriraj Hospital, Mahidol University
Bangkok, Bangkok, Thailand, 10700