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临床试验/IRCT20120915010841N18
IRCT20120915010841N18招募中1 期

Evaluation of Efficacy of intravenous Atropine in prevention of post spinal hypotension and bradycardia in cesarean section.

Hamedan University of Medical Sciences0 个研究点目标入组 88 人开始时间: 待定最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
入组人数
88

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 40 years(—)
性别
Female

入选标准

  • Satisfaction to participate in the project
  • Pregnant women aged 18 to 46
  • Pregnant women who underwent cesarean section under spinal anesthesia

排除标准

  • sensitivity to medications used
  • Patients who have failed spinal anesthesia and undergo general anesthesia
  • Lung disease, heart disease, asthma, fever, hypertension, preeclampsia and eclampsia, cardiac arrhythmia
  • Multiple pregnancies
  • HR resting more than 100 in minutes,
  • Beta-blocker intake

研究者

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