NCT00103922已完成3 期
A Randomized, 24-week, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Efficacy, Safety and Tolerability of ARIFLO® (15mg BID) in Patients With Chronic Obstructive Pulmonary Disease (COPD)
适应症
干预措施
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 600
- 试验地点
- 1
- 主要终点
- measure of lung function and quality of life in patients with COPD
研究概览
简要总结
This study was designed to determine if the investigational drug is effective and safe in individuals with COPD (chronic pulmonary disease)
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 40 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
研究组 & 干预措施
Arm 1
Experimental
干预措施: cilomilast (Drug)
结局指标
主要结局
measure of lung function and quality of life in patients with COPD
次要结局
- exacerbations in patients with COPD
研究者
研究点 (1)
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