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临床试验/CTRI/2018/12/016518
CTRI/2018/12/016518已完成4 期

Randomized double-blind comparison of phenylephrine and norepinephrine for treatment of post-spinal hypotension in parturients with fetal compromise

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

  • 1. Healthy females with singleton pregnancy undergoing emergency caesarean section for potential fetal compromise under spinal anaesthesia
  • 2. Non-reassuring fetal heart rate (FHR) status i.e. FHR more than 160 or less than 100 bpm
  • 3. FHR deceleration(variable or late), which fails to recover after uterine contraction has passed (type 2 dips)
  • 4. Meconium stained liquor with FHR abnormality or thick meconium stained liquor
  • 5. Cord prolapse
  • 6. Intra-uterine growth restriction
  • 7. Oligohydramnios
  • 8. Antepartum haemorrhage
  • 9. Dystocia
  • 10. Postmaturity
  • 11. Prematurity

排除标准

  • 1. Maternal complications e.g. pre-eclampsia, cardiovascular disease, cerebrovascular disease
  • 2. Multiple gestation
  • 3. Known fetal abnormality
  • 4. 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
  • 5. Maternal baseline SBP less than 100 mmHg
  • 6. Severely compromised fetus requiring immediate administration of general anaesthesia to mother
  • 7. Patients on monoamine oxidase inhibitors or tricyclic antidepressants
  • 8. 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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