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临床试验/ACTRN12608000487314
ACTRN12608000487314已完成未知

Can Heliox improve the sensation of breathlessness and increase exercise duration in chronic obstructive pulmonary disease; A prospective randomized trial.

Department of Respiratory Medicine, Repatriation General Hospital0 个研究点目标入组 15 人开始时间: 2008年9月30日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
15

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
40 Years 至 o limit(—)
性别
All

入选标准

  • Are aged over 40
  • Chronic Obstructive Pulmonary Disease (COPD) of at least Stage III as per the Global initiative for chronic Obstructive Lung Disease (GOLD) guidelines, Forced Expiratory Volume in the first second (FEV1) <= 50% predicted post bronchodilator.
  • Are able to give informed written consent prior to entering the study.
  • Can comply with scheduled visit and all study related activities

排除标准

  • Any clearly documented history of adult asthma or chronic respiratory disorders (e.g. primary bronchiectasis, pulmonary fibrosis or any clearly documented history of adult asthma or chronic respiratory disorders (e.g. primary bronchiectasis, pulmonary fibrosis, pneumoconiosis) other than COPD.
  • Any contraindication for Cardio Pulmonary Exercise Testing (CPET), as per American Thoracic Society and American College of Chest Physicians guidelines (ATS/ACCP 2003)
  • Participating in a research study or use of any investigational drug during this studys, pneumoconiosis) other than COPD.

研究者

发起方
Department of Respiratory Medicine, Repatriation General Hospital

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