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临床试验/CTRI/2021/02/031048
CTRI/2021/02/031048招募中4 期

Comparison of prophylactic infusions of phenylephrine and norepinephrine in parturients with fetal compromise undergoing caesarean section: a randomised double blind study

niversity College of Medical Sciences and Guru Teg Bahadur Hospital0 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
招募中
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

  • Healthy females with singleton pregnancy undergoing caesarean section for potential fetal compromise under spinal anaesthesia
  • Non-reassuring fetal heart rate (FHR) status i.e. FHR >160 or <100 bpm or abnormal FHR ( > 180 bpm) (As per the RCOG guidelines 2018)
  • FHR deceleration (variable or late), which fails to recover after uterine contraction has passed (type 2 dips)
  • Meconium stained liquor with FHR abnormality or thick meconium stained liquor
  • Intra-uterine growth restriction
  • Oligohydramnios
  • Antepartum haemorrhage
  • Postmaturity
  • Prematurity

排除标准

  • Maternal complications e.g. pre-eclampsia, 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
  • Severely compromised fetus requiring immediate administration of general anaesthesia to mother
  • Patients on monoamine oxidase inhibitors or tricyclic antidepressants
  • History suggestive 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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