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临床试验/CTRI/2020/03/023761
CTRI/2020/03/023761已完成3 期

A prospective, randomized double-blinded study to compare Phenylephrine andNorepinephrine infusion to prevent hypotension following Subarachnoid block in patients undergoing Caesarean delivery.

AIIMS Raipur0 个研究点目标入组 95 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
95

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

  • Grade 3 and 4 as per Lucas classification of urgency of caesarean section
  • Pregnant females undergoing Caesarean section under spinal anaesthesia
  • Age 18-35 years
  • ASA grade 2
  • Gestational age more than 37 weeks with singleton pregnancy

排除标准

  • Not consenting for the study
  • ASA grades 3,4
  • Body weight <50kgs, >100kgs
  • Height <140cm, >170cm
  • Any pregnancy complications like pregnancy-induced hypertension, gestational diabetes,abruptio placenta,
  • placenta previa
  • Any medical diseases like Diabetes mellitus, Hypertension, Cardiac diseases, Severe anemia, Peripheral
  • vascular diseases.
  • Failed subarachnoid block
  • Contraindication to Spinal Anaesthesia
  • Patients on monoamine oxidase inhibitors and anti-depressants
  • Spinal Deformities
  • Diagnosed preoperative fetal compromise

研究者

发起方
AIIMS Raipur

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