PACTR201803003123163
Completed
未知
Obstetric outcomes following immedicate versus delayed intravenous Oxytocin after amniotomy among parturients: A randomized clinical trial
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.
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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