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临床试验/ACTRN12613000988752
ACTRN12613000988752进行中(未招募)未知

To determine if clinically relevant and statistically significant improvements in asthma control questionnaire score can be achieved and sustained by monitoring bronchial hyperresponsiveness (BHR) to inhaled mannitol in individuals with asthma when compared to assessing spirometry alone.

Sydney Local Health District - Royal Prince Alfred Hospital0 个研究点目标入组 50 人开始时间: 2013年9月5日最近更新:
适应症

试验速览

阶段
未知
状态
进行中(未招募)
发起方
入组人数
50

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
Open (masking not used)

入排标准

年龄范围
18 Years 至 75 Years(—)
性别
All

入选标准

  • Males and females age 18-75 years
  • -Pre-bronchodilator FEV1 greater than or equal to 70% of predicted and greater than 1L
  • -A positive response to mannitol challenge (PD15 of less than 635mg)
  • -Prescribed ICS treatment after initial challenge
  • -Non-smokers; ex-smokers with less than 10 pack years and no cigarettes within the last 12 months
  • ACQ score greater than 0.75

排除标准

  • -Evidence of significant cardiovascular, haematological, hepatic, renal, neurological or psychiatric disease or any other major immunological or pulmonary disease other than asthma.
  • -Upper or lower respiratory tract infection within 2 weeks of the baseline visit, which may or may not have required a course of oral antibiotics
  • -Administration of an investigational drug in the preceding 4 months
  • -Subjects positive to mannitol that are being assessed as defence or police recruits

研究者

发起方
Sydney Local Health District - Royal Prince Alfred Hospital

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