跳至主要内容
临床试验/CTRI/2023/07/055528
CTRI/2023/07/055528尚未招募4 期

To compare bolus doses of nor epinephrine and phenylephrine for treatment of maternal hypotension undergoing emergency lower segment cesarean section under subarachnoid block : A Randomized Clinical Study. - NI

Dr Rajat Kathpal0 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
4 期
状态
尚未招募
发起方

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

  • Those parturients who will develop hypotension after subarachnoid block, with systolic blood pressure being <20% of the baseline value will be included in the study.

排除标准

  • Parturients with:-
  • 1.Fetal Abnormality.
  • 2.Preexisting or Pregnancy Induced Hypertension.
  • 3.Known Cardiovascular or Cerebrovascular Disease.
  • 4.Thrombocytopenia.
  • 5.Coagulopathy or any medical contraindication to spinal anesthesia.
  • 6.Weight <50 kg or >100kg.
  • 7.Height <140 cm or >180 cm.
  • 8.Parturient using monoamine oxidase inhibitors or tricyclic anti-depressants.
  • 9.Parturient allergic to study drug.
  • 10.Refusal of informed consent.

研究者

发起方
Dr Rajat Kathpal

相似试验

To compare effect of nor epinephrine and... | 临床试验