跳至主要内容
临床试验/NCT01785901
NCT01785901已完成不适用

The Asthma Control Rate Achieved by Budesonide/Formoterol in Clinical Practice in China

AstraZeneca2 个研究点 分布在 1 个国家目标入组 1,502 人开始时间: 2013年5月最近更新:
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

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

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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