DRKS00013938已完成不适用
TriOptimize: A prospective non-interventional Trial on COPD patients’ health related quality of life under a fixed LAMA/LABA/ICS triple therapy and characterization of determinants of treatment adherence - TriOptimize
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Chiesi GmbH
- 入组人数
- 2,623
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 with moderate to severe COPD (with and without asthma).
- •2) The doctor made the decision for a therapy with Trimbow® within the scope of its German approval, regardless of the present study.
- •3) Patients who have had at least one COPD exacerbation within the 12 months prior to starting treatment with Trimbow®.
- •4) Patients who are willing and able to give their written consent to the use of their pseudonymised personal data for the purposes of the present study.
排除标准
- •1) Patients who were hospitalized for a COPD exacerbation within the last 4 weeks prior to inclusion.
- •2) Participation in a clinical trial within the last 30 days before inclusion in the present NIS.
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