ISRCTN14411274进行中（未招募）未知
Assessment of an electronic system of the impact on inhaler skills and technique
niversity of Manchester0 个研究点目标入组 126 人开始时间: 2022年6月8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
- 126
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. Provision of signed and dated informed consent
- •2. Willingness to comply with the study procedures and confirmed availability for the study duration
- •3. Aged =16 years
- •4. Self-reported asthma diagnosis and currently receiving treatment
- •5. Regularly prescribed one of the following brands of inhaler and has been using it for at least 1-month prior to enrolment:
- •5.1. Fostair pMDI (100 mcg Beclometasone/ 6 mcg Formoterol per dose; 200 mcg Beclometasone/ 6mcg Formoterol per dose); Chiesi Ltd
- •5.2. Clenil Modulite pMDI (50 mcg, 100 mcg, 200 mcg or 250 mcg Beclometasone per dose); Chiesi Ltd
- •5.3. Trimbow pMDI (87 mcg Beclometasone, 5 mcg Formoterol, 9 mcg Glycopyrronium per dose); Chiesi Ltd
- •5.4. Seretide Evohaler pMDI (50 mcg Fluticasone/Salmeterol 25 mcg per dose; 125 mcg Fluticasone/Salmeterol 25 mcg per dose; 250 mcg Fluticasone/ Salmeterol 25 mcg per dose); GSK UK Ltd
- •5.5. Flixotide Evohaler pMDI (50 mcg Fluticasone per dose; 125 mcg Fluticasone per dose; 250 mcg Fluticasone per dose); GSK UK Ltd
- •6. Access to a smartphone or tablet device and willingness to use it to regularly assess inhaler technique for the study duration
排除标准
- •1. Using a spacer to assist with using their inhaler
- •2. Prescribed oral steroids for asthma in the preceding 1-month
- •3. Medication is not self-administered
- •4. Previous treatment for acute asthma in an IC
研究者
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