NL-OMON55983招募中不适用
A portable dyspnea RELIEF device for episodic breathlessness in COPD (PEP-buddy): effect on dyspnea severity and mechanism of action - RELIEF-study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 25
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
- 年龄范围
- 18 至 99（—）
入选标准
- •1. Age >=40 years 2. Read, understood and signed Informed Consent 3. COPD Gold
- •class II-IV/ B or E (FEV1<60% of predicted, CAT >=10 points) 4. Optimized
- •standard therapy according to the study physician 5. Episodic breathlessness
- •requiring intervention (i.e. taking rest during physical activities, as needed
- •inhalation medication, breathing techniques, as needed opioids) at least three
- •days per week
排除标准
- •1. Other severe disease causing episodic breathlessness
- •2. Life expectancy <= 3 months
- •3. Exacerbation of COPD 4 weeks prior to inclusion
- •4. Change in COPD management targeted at breathlessness 8 weeks prior to
- •5. Inability to use the PEP buddy device
- •6. Currently participating in another interventional clinical study
- •7. Any other conditions, which, in the opinion of the investigator would make
- •the patient unsuitable for inclusion, or could interfere with the patient
- •participating in or completing the study.
研究者
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