DRKS00031897已完成不适用
A prospective non-interventional study to assess quality of life and COPDsymptoms in patients with COPD on LAMA/LABA/ICS triple therapy withElebrato® Ellipta® - ELLLITHE, Study number: BC Be/20/ELE-NIS/01
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 931
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 one（—）
- 性别
- All
入选标准
- •1. Patients =18 years, with moderate to severe COPD (FEV1 =30% - <80%)
- •2. Decision for the therapy with Elebrato Ellipta was made in accordance with the current registration and independently from the participation in this NIS,
- •3. Patients with at least one COPD exacerbation within the last 12 months prior to starting treatment with Elebrato Ellipta,
- •4. Patients with a CAT = 10 prior to starting treatment with Elebrato Ellipta,
- •5. Patient treated with Elebrato Ellipta for the first time; this includes patients already on Elebrato Ellipta for a maximum of 4 weeks prior to enrolment into
- •this NIS, and whose COPD medication was not changed during this period,
- •6. Patients who are willing and able to give their written consent to the use of their pseudonymized personal information for the purposes of this study.
排除标准
- •1. Patients hospitalized due to COPD exacerbation within the last 4 weeks prior to enrolment,
- •2. Participation in a clinical trial within the last 30 days prior to inclusion in this NIS,
- •3. Any contraindication as per the SmPC of Elebrato Ellipta.
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