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Clinical Trials/PACTR201803003123163
PACTR201803003123163
Completed
未知

Obstetric outcomes following immedicate versus delayed intravenous Oxytocin after amniotomy among parturients: A randomized clinical trial

Kenyatta National Hospital0 sites202 target enrollmentFebruary 20, 2018

Overview

Phase
未知
Intervention
Not specified
Conditions
Pregnancy and Childbirth
Sponsor
Kenyatta National Hospital
Enrollment
202
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 20, 2018
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Pregnant mothers who:
  • 1\.Provide informed consent
  • 2\.Have intact membranes at 37 completed weeks or greater.
  • 3\. Have singleton vertex pregnancies.
  • 4\.Require ARM (at cervical dilatation of 4 cm) for example due to inadequate uterine contractions or poor progress in labour.

Exclusion Criteria

  • Pregnant mothers in labour with:
  • 1\.Multiple gestation.
  • 2\.Malpresentation (non\-vertex)
  • 3\.Previously had uterine surgery.
  • 4\.Virally unsuppressed HIV infection.
  • 5\.Non\-reassuring fetal status prior to amniotomy.
  • 6\.Post amniotomy meconium stained liquor, fetal tachycardia, fetal bradycardia, umbilical cord or limb prolapse.
  • 7\.Antepartum hemorrhage due to any cause.
  • 8\.Hypertensive disease, Diabetes and Cardiac disease in pregnancy.
  • 9\.Known/ suspected fetal growth restriction.

Outcomes

Primary Outcomes

Not specified

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