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临床试验/IRCT201601238768N4
IRCT201601238768N4已完成2 期

Comparison between different prophylactic & therapeutic phenylephrine regimenes in reducing maternal hypotention after induction of spinal anesthesia in caesarean section

Vice chancellor for Research and Technology, Hamadan University Of Medical Sciences0 个研究点目标入组 120 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
120

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
16 years 至 50 years(—)
性别
Female

入选标准

  • All of the ASA 1 healthy term parturients referring to Fatemieh hospital candidate for Cesarean section were included in the study.
  • Exclusion criteria: chronic hypertension; pre eclampsia; twin pregnancy;, preterm labor; allergy to drugs; cardiovascular disease; renal disease and previous abdominal surgeries with adhesion band and fibrosis.

排除标准

  • 未提供

研究者

发起方
Vice chancellor for Research and Technology, Hamadan University Of Medical Sciences

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