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临床试验/ACTRN12616000884404
ACTRN12616000884404招募中4 期

The incidence of maternal hypotension during elective caesarean delivery under spinal anesthesia in healthy ASA I pregnant women: comparison of intravenous ondansetron, continuous infusion of phenylephrine and ondansetron plus continuous infusion of phenylephrine with placebo. A double blind, randomized, placebo controlled trial.

niversity Hospital Gregorio Maranon0 个研究点目标入组 280 人开始时间: 2016年7月5日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
280

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
20 Years 至 45 Years(—)
性别
Female

入选标准

  • American Society of Anaesthesiologists class I women scheduled for lower segment caesarean delivery under spinal anesthesia enrolled during anesthesia consultation or early in the third trimester.
  • Written informed consent must be obtained from all patients to participate in this study.

排除标准

  • Exclusion criteria included refusal to participate, contraindication to spinal anaesthesia, age less than 20 years or greater than 45 years, obesity (body mass index (BMI) at term greater than 30 kg/m2), any ASA physical status not equal to 1, previous fluid therapy and history of allergy to or side effects from ondansetron or phenylephrine.

研究者

发起方
niversity Hospital Gregorio Maranon

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