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临床试验/NCT01699594
NCT01699594已完成不适用

Allergen Induced Increase in Indirect Non-allergic Bronchial Reactivity

University of Saskatchewan1 个研究点 分布在 1 个国家目标入组 11 人开始时间: 2012年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
11
试验地点
1
主要终点
Change from baseline in airway responsiveness three hours after allergen exposure

研究概览

简要总结

Exposure to allergens changes the way the airway responds to some stimuli (methacholine). The investigators will look at whether or not exposure to allergens changes the way the airway responds to a different stimuli (mannitol) and compare that with the known stimuli (methacholine).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • mild, allergic asthma
  • FEV1 greater than 70% predicted
  • methacholine PC20 less than or equal to 16mg/ml

排除标准

  • known sensitivity to mannitol or other excipient
  • diagnosis of any other respiratory or non respiratory disease/disorder that would preclude the individual from participating
  • recent thoracic, abdominal or eye surgery
  • recent allergen exposure (4 weeks), respiratory infection (6 weeks)
  • current immunotherapy
  • pregnancy
  • history of anaphylaxis
  • use of asthma therapies other than short acting beta agonist

研究组 & 干预措施

Mannitol

Experimental

This arm will assess the allergen induced change in airway responsiveness to mannitol bronchoprovocation.

干预措施: Mannitol (Drug)

Methacholine Chloride

Active Comparator

This arm will assess the allergen induced change in airway responsiveness to methacholine bronchoprovocation.

干预措施: Methacholine Chloride (Drug)

结局指标

主要结局

Change from baseline in airway responsiveness three hours after allergen exposure

时间窗: Change from Baseline at 3 hours

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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