ACTRN12612000996864已完成4 期
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 个研究点目标入组 180 人开始时间: 2012年9月17日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 180
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Prevention
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit(—)
- 性别
- Female
入选标准
- •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
排除标准
- •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
- •9.Excessive shivering that makes blood pressure
- •monitoring unreliable
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