跳至主要内容
临床试验/NCT02622243
NCT02622243已完成4 期

Duration of Bronchoprotection of the Long Acting Muscarinic Antagonists Tiotropium and Glycopyrronium Against Methacholine Induced Bronchoconstriction

University of Saskatchewan1 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2015年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
13
试验地点
1
主要终点
Change from baseline methacholine bronchoprotection at 96 hours

研究概览

简要总结

The study will assess the duration of protection of single doses of 2 different long acting muscarinic antagonists against methacholine induced bronchoconstriction.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • male or female asthmatics > 19 years of age
  • baseline methacholine PC20 less than or equal to 4mg/ml
  • baseline lung function >65% predicted
  • non-smoker and less than 10 pack year smoking history

排除标准

  • use of anticholinergic within 30 days of Visit 1
  • poorly controlled asthma
  • pregnant or nursing
  • respiratory illness within 4 weeks of Visit 1
  • exposure to an agent that triggered asthma worsening (e.g. allergen) within 4 weeks of Visit 1

研究组 & 干预措施

tiotropium

Experimental

2 inhalations of 2.5mcg/inhalation tiotropium from Respimat inhaler and 1 inhalation of placebo from Breezehaler 1 hour prior to methacholine challenge

干预措施: Tiotropium (Drug)

tiotropium

Experimental

2 inhalations of 2.5mcg/inhalation tiotropium from Respimat inhaler and 1 inhalation of placebo from Breezehaler 1 hour prior to methacholine challenge

干预措施: Respimat (Device)

tiotropium

Experimental

2 inhalations of 2.5mcg/inhalation tiotropium from Respimat inhaler and 1 inhalation of placebo from Breezehaler 1 hour prior to methacholine challenge

干预措施: Breezehaler (Device)

glycopyrronium

Experimental

1 inhalation of 50mcg glycopyrronium from Breezehaler and 2 inhalations from placebo Respimat inhaler 1 hour prior to methacholine challenge

干预措施: glycopyrronium (Drug)

glycopyrronium

Experimental

1 inhalation of 50mcg glycopyrronium from Breezehaler and 2 inhalations from placebo Respimat inhaler 1 hour prior to methacholine challenge

干预措施: Respimat (Device)

glycopyrronium

Experimental

1 inhalation of 50mcg glycopyrronium from Breezehaler and 2 inhalations from placebo Respimat inhaler 1 hour prior to methacholine challenge

干预措施: Breezehaler (Device)

结局指标

主要结局

Change from baseline methacholine bronchoprotection at 96 hours

时间窗: pre treatment versus 96 hour post treatment

assessed by dose shift of geometric mean methacholine PC20 data

次要结局

  • Change from baseline methacholine bronchoprotection at 1 hour(pre treatment versus 1 hour post treatment)
  • Change from baseline methacholine bronchoprotection at 24 hours(pre treatment versus 24 hours post treatment)
  • Change from baseline methacholine bronchoprotection at 48 hours(pre treatment versus 48 hours post treatment)
  • Change from baseline methacholine bronchoprotection at 72 hours(pre treatment versus 72 hours post treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Don Cockcroft

Professor

University of Saskatchewan

研究点 (1)

Loading locations...

相似试验