JPRN-UMIN000011462招募中未知
The clinical study of the budesonide/formoterol combination drug additional dosage in the perioperative period in a lung cancer patient with COPD. - The clinical study of the budesonide/formoterol combination drug additional dosage in the perioperative period in a lung cancer patient with COPD.
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 入组人数
- 40
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
- 20years-old 至 ot applicable（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1)Patient that there is ICS/LABA mixing medicine in pre-administering within four weeks 2)Patient where exacerbation of COPD was admitted within four weeks 3)Patient that there is past of hypersensitivity in atropine, the kind edge material or tiotropium, budesonide or formoterol 4)Patient who has chronic ailments of lungs, heart, kidney, liver, and blood, etc. 5)Patient who has previous history of adrenal cortical insufficiency or accentuation syndrome 6)Patient who has glaucoma 7)Patient who has dysuria such as dysuria by enlarged prostate 8)Case who judged doctor in charge targets and it is improper
研究者
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招募中
不适用
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