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临床试验/TCTR20200213001
TCTR20200213001尚未招募不适用

Minimum effective volume of crystalloid to prevent spinal induced hypotension during elective cesarean delivery: An up-down sequential allocation design.

Department of Anesthesiology0 个研究点目标入组 100 人开始时间: 2020年2月13日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 N/A (No limit)(—)
性别
Female

入选标准

  • Singleton term pregnancy
  • Elective cesarean delivery
  • American Society of Anesthesiology classification I-II

排除标准

  • Pregnant woman who has hypertensive disorder
  • Cardiac pathologies/ Fluid overload and contraindicated for fluid loading
  • Pregnant woman with extreme height (< 150 cm, > 190 cm)
  • BMI > 35 kg/m2 at the time of delivery
  • Patient who has inadequate spinal anesthesia or high spinal/ total spinal anesthesia
  • Refusal to participate the study

研究者

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