ACTRN12609000186257Completed未知
Induction of labour in nulliparous women with an unfavourable cervix: A Randomised Controlled Trial of Prostaglandin E2 Intravaginal Gel, a Double Balloon Catheter (Atard Ripener Device (ARD)) and the Foley Catheter
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Enrollment
- 330
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- Randomised controlled trial
- Primary Purpose
- Treatment
- Masking
- Open (masking not used)
Eligibility Criteria
- Ages
- 16 Years to o limit (—)
- Sex
- Female
Inclusion Criteria
- •Nulliparous women.
- •Over 36 weeks’ gestation.
- •Singleton fetus in cephalic presentation. Intact membranes.
- •Modified Bishop score of 0 to 4
Exclusion Criteria
- •Previous uterine surgery
- •Low-lying placenta
- •Any active or purulent infection of the lower vaginal tract
- •Abnormal pre-induction fetal heart rate (FHR) tracing
Investigators
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