ACTRN12622001342707
Recruiting
Phase 1
A Randomised Controlled Trial of Easing Oxytocin in Early Labour: Outcomes for Mothers and Babies - a feasibility study
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- abour
- Sponsor
- Royal Prince Alfred Hospital
- Enrollment
- 100
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Age \> 18 years
- •2\. Planned induction of labour using oxytocin
Exclusion Criteria
- •1\. A fetus with a known major anomaly
- •2\. Red\-Zone” (abnormal) fetal cardiotocograph according to NSW Health classification
- •3\. Fetal breech, brow or face presentation
- •4\. Clinical suspicion of cephalopelvic disproportion
- •5\. Known or suspected chorioamnionitis
- •6\. Intrapartum haemorrhage greater than 50mL
- •7\. Intrapartum pyrexia greater than 38C
- •8\. Fetal scalp pH less than 7\.25 or lactate greater than 4
- •9\. Pre\-existing maternal diabetes
- •10\. Previous caesarean section
Outcomes
Primary Outcomes
Not specified
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abor induction for premature rupture of membranespremature rupture of membranes at term.Preterm spontaneous labour with preterm deliveryIRCT2016042627615N1Vice Chancellor for Research, Mashhad University of Medical Sciences86