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临床试验/CTRI/2022/12/047845
CTRI/2022/12/047845尚未招募未知

A study to compare the effect of prophylactic infusion of two different doses of phenylephrine on maternal hypotension and neonatal outcome in females undergoing cesarean section under spinal anaesthesia.

Department of Anaesthesia0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募

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

入选标准

  • 1.Patients with physical status ASA grade I or II.
  • 2.All patients giving written informed consent.
  • 3.Patients with gestation age > 36 weeks posted for elective caesarean delivery under spinal anaesthesia.
  • 4.Patients belonging to age group of 18 to 35 years.

排除标准

  • 1.Parturients with complications like risk of excessive bleeding (placenta previa, prolonged labor, abnormal presentation, multiple gestation)
  • 2.Patients with pre-existing or pregnancy induced hypertension or maternal SBP < 100mm Hg.
  • 3.Patients with cardiovascular disease, cerebrovascular disease, severe anemia or diabetes.
  • 4.Patients with known fetal abnormalities.
  • 5.Patients with contraindication to spinal anaesthesia.
  • 6.Patients with known allergy to phenylephrine
  • 7.Patients with inability or refusal to give informed consent

研究者

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