ISRCTN55359097已完成未知
A method comparison study comparing intra- and inter-user reproducibility of FeNO measurement using the NObreath® V2
Bedfont® Scientific Ltd0 个研究点目标入组 186 人开始时间: 2020年9月4日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 186
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Aged 7 years or above
- •2. If on allergy immunotherapy treatment this must be a stable regimen during the study
- •3. Be capable of producing valid FeNO measurements via the NObreath®
- •4. Be capable of performing spirometry in accordance with ATS/ERS criteria
排除标准
- •1. Hospitalisation related to asthma in the past 6 months
- •2. Use of oral corticosteroid in the 4 weeks prior to visit 1
- •3. Use of biological therapies e.g. mepolizumab in 12 weeks prior to visit 1
- •4. Other respiratory diseases e.g. COPD or cystic fibrosis
- •5. Known intolerance to inhaled corticosteroids or salbutamol
- •6. Cardiovascular conditions:
- •6.1. Coronary artery disease
- •6.2. High blood pressure
- •6.3. Heart failure
- •6.4. Diagnosed abnormality of heart rhythm
- •7. A smoking history of >10 packs per year
- •8. Pregnant
研究者
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