NCT03012737终止不适用
Palliation of Dyspnea With Mouth Piece Ventilation
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 22
- 试验地点
- 4
- 主要终点
- Change in dyspnea after initial use of MPV
研究概览
简要总结
An uncontrolled feasibility study on using mouth piece ventilation in palliation of dyspnea in subjects with incurable advanced disease. Subjects are recruited from a local Hospice and from oncology ward. The main outcomes are the compliance of the subjects with the treatment and alleviation of dyspnea during the treatment period.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •at least moderate dyspnea (NRS = Numeric Rating Scale ≥ 4)
- •incurable advanced disease
- •able to understand the study and to give informed consent
- •would not gain from intensive care or resuscitation according to the treating physician
排除标准
- •unable to participate and use MPV due to e.g. delirium or lack of co-operation
- •the cause of the dyspnea can be succesfully treated
- •unable to give informed consent
结局指标
主要结局
Change in dyspnea after initial use of MPV
时间窗: 5 - 60 min
次要结局
- Proportion of subjects gaining from MPV(24 hours)
- Change in dyspnea after 24 hours of using MPV(24 hours)
- Proportion of subjects having side-effects or not being compliant with MPV(24 hours)
- Proportion of subjects willing to continue on MPV after the intervention(24 hours)
研究者
Lauri Lehtimäki
Associate professor
Tampere University Hospital
研究点 (4)
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