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Induction of Labour with a Foley catheter or Misoprostol at Term

Phase 3
Completed
Conditions
induction of labour
10010273
Registration Number
NL-OMON39523
Lead Sponsor
Academisch Medisch Centrum
Brief Summary

Trial is onging in other countries

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
1869
Inclusion Criteria

Term pregnancy (>=37 weeks of pregnancy)
Scheduled for induction of labour
Vital singleton pregnancy
Intact membranes
Unfavourable cervix (Bishop score < 6)
Cephalic presentation

Exclusion Criteria

Previous caesarean section
Placenta praevia
Hypersensitivity for one of the products used for induction
Maternal age <18 years
Lethal congenital anomaie

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The primary outcome will be a composite of complications of uterine<br /><br>hyperstimulation, i.e. asphyxia and fluxus post partum. We will also compare<br /><br>the instrumental delivery rate.</p><br>
Secondary Outcome Measures
NameTimeMethod
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