ACTRN12612000996864
Completed
Phase 4
A randomised clinical trial at the time of spinal anaesthesia for elective caesarean section to investigate the effect of equipotent phenylephrine and metaraminol infusions on neonatal outcome
King Edward Memorial Hospital for Women0 sites180 target enrollmentSeptember 17, 2012
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- eonatal acid-base status.
- Sponsor
- King Edward Memorial Hospital for Women
- Enrollment
- 180
- Status
- Completed
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Women undergoing elective Caesarean section
- •under spinal or combined spinal epidural (CSE)
- •anaesthesia
- •2\.Gestational age \> 37 weeks
- •3\.Singleton pregnancy
- •4\.ASA I and II
- •5\.Height between 150 and 190 cm
- •6\.Weight between 50 and 115 kg
- •7\.Body mass index (BMI) between 20 and 35 kg/m2
Exclusion Criteria
- •1\.Contraindication to spinal or CSE anaesthesia
- •2\.Diabetes mellitus
- •3\.Preeclampsia, pregnancy\-induced hypertension or
- •essential hypertension
- •4\.Cardiovascular or cerebrovascular disease
- •5\.Fetal abnormality or intrauterine growth restriction
- •6\.Failure to establish block to cold to T4
- •7\.Supplementary epidural anaesthesia prior to
- •delivery of the baby
- •8\.Conversion to general anaesthesia
Outcomes
Primary Outcomes
Not specified
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