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临床试验/CTRI/2020/04/024801
CTRI/2020/04/024801已完成不适用

Comparision of efficacy of two different bolus doses of norepinephrine as prophylactic to prevent postspinal hypotension during elective caesarean section.

Kasturba medical college1 个研究点 分布在 1 个国家目标入组 84 人开始时间: 2020年2月5日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
84
试验地点
1
主要终点
Success of prophylactic iv bolus of norepinephrine to maintain SBP at or above 80% of baseline

研究概览

简要总结

Comparison of efficacy of two different bolus doses of norepinephrine as prophylactic to prevent postspinal hypotension during elective caesarean section.

This study aims to compare the efficacy of two different bolus dosages of norepinephrine in effectively reducing the incidence of post spinal hypotension during elective caesarean section thereby improves maternal and fetal outcomes.

研究设计

研究类型
Interventional
分配方式
Not Applicable
盲法
Not Applicable

入排标准

年龄范围
18.00 Year(s) 至 45.00 Year(s)(—)
性别
Female

入选标准

  • 1.Pregnant females undergoing elective caesarean section under spinal anaesthesia.
  • 2.Full term pregnancy.
  • 3.Singleton pregnancy.
  • 4.BP range 90-140 mmHg 5.ASA physical status II 6.Age 18 years and older.
  • 7.Weight between 50 and 100 kg.
  • 8.Height between 150 and 170 cm.

排除标准

  • Patient refusal.
  • Hypertension, cardiovascular or cerebrovascular disease.
  • Fetal abnormalities.
  • Diabetes (excluding gestational diabetes).

结局指标

主要结局

Success of prophylactic iv bolus of norepinephrine to maintain SBP at or above 80% of baseline

时间窗: from induction to delivery of foetus

次要结局

  • 1.Hypertension(2.Bradycardia)

研究者

申办方类型
Private medical college

研究点 (1)

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