NL-OMON46686已完成不适用
Pulmonary RehabIlitation with Nasal-high-flow-support in COPD and Effectiveness: The PRINCE study - PR with NHF in COPD and Effectiveness
CIRO+ Horn0 个研究点目标入组 80 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 80
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
- •- - Patients with COPD with hypoxia which at least demand 1 liter oxygen/min during baseline.
- •- Clinical stable on the basis of clinical picture by the chest physician.
- •- Documented desaturation during exercise, which demands at least 2 liters oxygen/min to correct.
- •- Permission for voluntary participation. Patient will be asked during the start of their rehabilitation program and have to sign an informed consent. Patients have the right to withdraw from the study without any negative consequences on their rehabilitation.
- •- Attending the regular rehabilitation program in CIRO+.
排除标准
- •- Lack of motivation for voluntary participation in the present study.
- •- Not capable to understand the instruction of the NHF oxygen delivery system
- •- Outpatient pulmonary rehabilitation program in a hospital which is part of the CIRO network.
- •- Not capable to perform cycle tests, walk tests and/or endurance training on a cycle ergometer and treadmill.
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