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Clinical Trials/ISRCTN13667534
ISRCTN13667534
Completed
Not Applicable

To evaluate the effectiveness of the use of an IntraUterine Pressure Catheter (IUPC) in comparison to external monitoring of uterine activity during (I) augmentation after arrest of labor, or (II) induction of labour with intravenous oxytocin. Does the potentially more accurate monitoring of uterine activity with IUPC lead to a better outcome of labour and delivery in a study that randomises the use of an IUPC?

Academic Medical Centre (AMC) (Netherlands)0 sites1,350 target enrollmentDecember 20, 2005
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ConditionsPregnancy, labourPregnancy and ChildbirthLabour

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pregnancy, labour
Sponsor
Academic Medical Centre (AMC) (Netherlands)
Enrollment
1350
Status
Completed
Last Updated
11 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 20, 2005
End Date
TBD
Last Updated
11 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Academic Medical Centre (AMC) (Netherlands)

Eligibility Criteria

Inclusion Criteria

  • •Women with the indication to induce labour or to stimulate the contractions with intravenous oxytocin in case of arrest of labour.

Exclusion Criteria

  • •1\. Women with a history of caesarean section
  • •2\. Gestational age less than 36 weeks
  • •3\. Intrauterine foetal death
  • •4\. Breech presentation
  • •5\. Multiple pregnancy
  • •6\. Maternal age greater than 18 years
  • •7\. Human immunodeficiency virus (HIV) or hepatitis B infection
  • •8\. Intrauterine infection
  • •9\. Contraindication for amniotomy
  • •10\. Participation in another randomised controlled trial

Outcomes

Primary Outcomes

Not specified

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