NCT00215397已完成2 期
Study in Patients With Asthma
Dey4 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2005年9月22日最近更新:
适应症
相关药物
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 16
- 试验地点
- 4
- 主要终点
- The primary outcome variable is the measure of lung function.
研究概览
简要总结
The purpose of this study is to determine which dose of the investigational drug is the most safe and effective in the treatment of asthma compared to the control drug.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Double
入排标准
- 年龄范围
- 5 Years 至 70 Years（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with a history of asthma
排除标准
- •Current asthma exacerbation or recent asthma exacerbation, requiring hospitalization
- •History of smoking
- •Debilitating systemic and/or life-threatening diseases.
结局指标
主要结局
The primary outcome variable is the measure of lung function.
次要结局
- Secondary outcomes include change in lung function, as well as in vital signs.
- Physical exams, AE reporting, etc.
研究者
研究点 (4)
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