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临床试验/TCTR20201223006
TCTR20201223006尚未招募2 期

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

Faculty of medicine Ramathibodi hospital, Mahidol university0 个研究点目标入组 100 人开始时间: 2020年12月23日最近更新:
适应症

试验速览

阶段
2 期
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 50 Years(—)
性别
Female

入选标准

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

排除标准

  • History of hypertensive disorder
  • Gestational age less than 37 weeks
  • History of cardiovascular disease
  • History of morbid obesity (Pre-pregnancy BMI > 35 kg/m2)
  • Height less than 150 cm or more than 190 cm
  • Inadequate or failed spinal anesthesia
  • High or total spinal anesthesia

研究者

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