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临床试验/CTRI/2016/12/007542
CTRI/2016/12/007542已完成4 期

Comparison of potency of norepinephrine and phenylephrine bolus doses for treatment of post-spinal hypotension during elective caesarean section

niversity College of Medical Sciences and Guru Teg Bahadur Hospital0 个研究点目标入组 100 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
100

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

  • Healthy females with term, uncomplicated, singleton pregnancy undergoing elective caesarean section under spinal anaesthesia

排除标准

  • Maternal complications e.g. diabetes, pre-eclampsia, other cardiovascular disease, cerebrovascular disease; multiple gestation; known fetal abnormality; patients with absolute or relative contra-indications for spinal anaesthesia e.g. infection in lumbar area, coagulation abnormalities, autonomic neuropathy, spinal deformities, other neurological diseases; hypovolemia due to any cause; maternal baseline SBP less than 100 mmHg; patients on monoamine oxidase inhibitors or tricyclic antidepressants; presence of mesenteric or peripheral vascular thrombosis

研究者

发起方
niversity College of Medical Sciences and Guru Teg Bahadur Hospital

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