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临床试验/ISRCTN25106564
ISRCTN25106564已完成未知

In-exsufflation mechanics in intubated patients: a randomized trial

Philips Respironics (France)0 个研究点目标入组 67 人开始时间: 2013年11月26日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
67

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

性别
All

入选标准

  • 1. Patient ventilated on endotracheal tube for less than 7 days
  • 2. Duration of mechanical ventilation predicted > 48h; 1. Patient ventilated on endotracheal tube for less than 7 days
  • 2. Duration of mechanical ventilation predicted > 48h

排除标准

  • 1. Pre-existing neuromuscular pathology, suspected or proven
  • 2. State of shock uncontrolled defined by the administration of norepinephrine or adrenaline at a dose> 0.3 mcg/kg/min
  • 3. Moderate to severe acute respiratory distress syndrome (ARDS) defined by a PaO2/FiO2 ratio <200 mmHg
  • 4. Undrained pneumothorax
  • 5. Hemoptysis active or less than 15 days
  • 6. Intracranial hypertension
  • 7. Decision to limit or stop the treatment
  • 8. Pregnancy
  • 9. Unable to follow study related procedures as explained by the investigator
  • 10. Minor patient; 1. Pre-existing neuromuscular pathology, suspected or proven
  • 2. State of shock uncontrolled defined by the administration of norepinephrine or adrenaline at a dose> 0.3 mcg/kg/min
  • 3. Moderate to severe acute respiratory distress syndrome (ARDS) defined by a PaO2/FiO2 ratio <200 mmHg
  • 4. Undrained pneumothorax
  • 5. Hemoptysis active or less than 15 days
  • 6. Intracranial hypertension
  • 7. Decision to limit or stop the treatment
  • 8. Pregnancy
  • 9. Unable to follow study related procedures as explained by the investigator
  • 10. Minor patient

研究者

发起方
Philips Respironics (France)

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