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Randomized Control Trial between Two Hourly Oral Misoprostol and Propess for Induction of Labor

Phase 2
Withdrawn
Conditions
Induction of labor.
Reproductive Health and Childbirth - Fetal medicine and complications of pregnancy
Registration Number
ACTRN12613000479707
Lead Sponsor
King Fahad Armed Forces Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Withdrawn
Sex
Female
Target Recruitment
200
Inclusion Criteria

1.Singleton pregnancy for induction of labor
2.No contraindication to either drug
3.Bishop score <6
4.Documented nonreactive stress test (NST)
5.Written informed consent

Exclusion Criteria

1.<34 weeks gestation
2.Severe pregnancy induced hypertension
3.Previous C/S or other uterine surgery
4.Parity 4 and more
5.Current uterine contractions

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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