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临床试验/EUCTR2005-003612-30-GB
EUCTR2005-003612-30-GB进行中(未招募)1 期

A comparison of Helium-oxygen mixture (Heliox) with an oxygen-air mixture in reducing the work of breathing during weaning from mechanical ventilation. - Heliox and weaning

Barts and the London NHS Trust0 个研究点目标入组 0 人开始时间: 2005年10月25日最近更新:
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试验速览

阶段
1 期
状态
进行中(未招募)
发起方

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
All

入选标准

  • Patient will be defined as ready for weaning with CPAP
  • ifFailed a spontaneous breathing trial
  • Pressure support ventilation < 10cmH2O
  • Underlying respiratory failure improving
  • No upper airway obstruction or bronchospasm
  • Not receiving continuous IV sedation
  • Not receiving vasoactive agents
  • FiO2 < 0.4 and
  • PEEP< 10 cm H2O and
  • Fully conscious
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Inadequate analgesia
  • Participation in other intervention trials in the past 30 days
  • Refusal of consent from the patient or assent from the next of kin

研究者

发起方
Barts and the London NHS Trust

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