跳至主要内容
临床试验/EUCTR2008-005660-13-GB
EUCTR2008-005660-13-GB进行中(未招募)不适用

COPD exacerbation - Heliox Therapy - AssessmentHeliox vs. Medical Air in Acute Exacerbation of Chronic Obstructive Pulmonary Disease: A Pilot Randomised Controlled Trial - Pilot CHeTA

BOC Ltd.0 个研究点目标入组 24 人开始时间: 2008年10月17日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
24

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

  • Be admitted to ED with a clinical diagnosis of an acute exacerbation of COPD
  • (acute onset of a sustained worsening of the patient’s symptoms from their usual
  • stable state which is beyond normal day-to-day variations).
  • Have a Past Medical History of a diagnosis of COPD
  • Age > 40 years.
  • After initial nebulisation have two of: RR>30, HR>100, purulent
  • 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

  • Have left ventricular failure.
  • Unable to give informed consent.
  • Clinical anticipation of intubation or non-invasive ventilation before randomisation.
  • Have participated in this trial before.
  • Participation in any investigational drug study within 4 weeks preceding or during this study period.
  • Clinical suspicion of large consolidation.
  • Encephalopathic

研究者

发起方
BOC Ltd.

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