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临床试验/EUCTR2013-005572-17-NL
EUCTR2013-005572-17-NL进行中(未招募)不适用

Optimizing propofol dosing for (preterm) newborn infants that needendotracheal intubation - NEOPROP2

Erasmus Medical Center0 个研究点开始时间: 2014年3月19日最近更新:
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相关药物

试验速览

阶段
不适用
状态
进行中(未招募)

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • All neonates admitted to the participating intensive care units:
  • - Less than 28 days postnatal age
  • - Who need endotracheal intubation
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 160
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patients with:
  • - Major congenital anomalies or neurological disorders,
  • - Neonates with an abnormal upper airway,
  • - Those receiving continuous sedatives or opioids, and
  • - Those whose mothers received sedatives or opioids before or during
  • delivery will be excluded during the first 2 days of life
  • - Those who previously participated in the study

研究者

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