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Clinical Trials/ACTRN12611000172909
ACTRN12611000172909
Completed
未知

on-reassuring fetal status assessed by the addition of lactate measurement, compared with fetal heart rate by cardiotocography-only, to reduce caesarean section rates.

Prof Christine East0 sites600 target enrollmentFebruary 15, 2011
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ConditionsCaesarean sectionNon-reassuring fetal statusPublic Health - Other public healthReproductive Health and Childbirth - Childbirth and postnatal careReproductive Health and Childbirth - Fetal medicine and complications of pregnancy

Overview

Phase
未知
Intervention
Not specified
Conditions
Caesarean section
Sponsor
Prof Christine East
Enrollment
600
Status
Completed
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 15, 2011
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Prof Christine East

Eligibility Criteria

Inclusion Criteria

  • •Greater than or equal to 37 weeks gestation
  • •Non\-reassuring fetal heart rate pattern

Exclusion Criteria

  • •Contraindication to fetal scalp blood sampling, including known HIV and Hepatitis B or C
  • •Planned caesarean section
  • •Chorioamnionitis requiring urgent delivery
  • •Known significant fetal anomaly

Outcomes

Primary Outcomes

Not specified

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