NCT01785901已完成不适用
The Asthma Control Rate Achieved by Budesonide/Formoterol in Clinical Practice in China
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- AstraZeneca
- 入组人数
- 1,502
- 试验地点
- 2
- 主要终点
- The rate of controlled and partly controlled asthma according to the definition of Global Initiative for Asthma
研究概览
简要总结
This is a multi-centre, cross-sectional study planned to be conducted in China. The study aims to observe about 1500 asthma patients who have already received budesonide/formoterol combination treatment by physicians' determination and whose medications are aligned with the package insert of budesonide/formoterol approved in China.
详细描述
The asthma control rate achieved by budesonide/formoterol in clinical practice in China.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Cross Sectional
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
- •Clinical diagnosis of asthma at least 6 months;
- •Prescribed with budesonide/formoterol treatment at least 3 months before enrolled;
- •Has used the same maintenance dose of budesonide/formoterol for at least 4 weeks before enrolled.
排除标准
- •Participation in any clinical study within 3 months;
- •Have COPD history/suspicious COPD;
- •≥ 10 pack years of smoking history
- •Used any other asthma maintenance medication accompanied with budesonide/formoterol within 3 months before enrolled
- •With asthma exacerbation (defined as asthma symptom deterioration resulting oral/rectal/parenteral GCS medication or emergency room treatment or hospitalisation) within 4 weeks before enrolled
结局指标
主要结局
The rate of controlled and partly controlled asthma according to the definition of Global Initiative for Asthma
时间窗: one day
次要结局
- The rate of completely controlled and well controlled asthma according to Asthma Control Test's score(one day)
- The average frequency of reliever use in previous week(one day)
研究者
研究点 (2)
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