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临床试验/NCT04245891
NCT04245891已完成不适用

Neonatal Evaluation of Norepinephrine Infusion in Spinal Anesthesia for Cesarean Section

Centre Hospitalier Universitaire de Nīmes1 个研究点 分布在 1 个国家目标入组 265 人开始时间: 2016年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
265
试验地点
1
主要终点
lactate level

研究概览

简要总结

This retrospective study aims to evaluate the fate of children born by cesarean section under spinal anesthesia with or without norepinephrine as vasopressor support for anesthesia. The main objective is to compare the initial Apgar score. The records of patients who received norepinephrine are compared to those without norepinephrine. To limit the biases of this type of study, the investigators will apply a propensity score that will include as a variable: age, ASA score, comorbidity, urgency. The patients analysed correspond to the period 2016-2017.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • age > 18
  • Spinal Anesthesia for Cesarean Section

排除标准

  • sub epidural cesarean section
  • contraindication to spinal anesthesia (allergy, severe heart disease, coagulopathy)

结局指标

主要结局

lactate level

时间窗: Just after the birth of the newborn baby

The primary endpoint is the Umbilical Cord Lactate levels

次要结局

  • Umbilical Cord venous PH(Just after the birth)
  • maternal arterial tension during cesarean section(0, 5,10,15, 20 25, 30,35,40 minutes after spinal anesthesia)
  • incidences of mother nausea and vomiting(from beginning to cesarean section end)
  • use of vasopressors(from beginning to cesarean section end)
  • APGAR Score(1, 5 and 10 minutes after birth)
  • Umbilical Cord arterial PH(Just after the birth)

研究者

发起方
Centre Hospitalier Universitaire de Nīmes
申办方类型
Other
责任方
Sponsor

研究点 (1)

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