NCT00660114已完成不适用
A Non-Interventional Study of Cough Variant Asthma Treatment With Pulmicort®Respules® in Patient Aged 5-Year Old or Younger in Outpatient Department
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
- 914
- 试验地点
- 1
- 主要终点
- Patient Symptom Score
研究概览
简要总结
This open label, non-interventional study is to show the efficacy of Pulmicort®Respules® in cough variant asthma in patient aged 5-year old or younger in outpatient department
研究设计
- 研究类型
- Observational
- 时间视角
- Prospective
入排标准
- 年龄范围
- — 至 5 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Provision of informed consent
- •Patient who has been prescribed Pulmicort® Respules® according to physician's judgement, irrespective of the inclusion in the study.
- •The usage of Pulmicort® Respules® follows local authorised package insert.
排除标准
- •Allergy to any ingredient of Pulmicort® Respules®
- •With history of Leukotriene Modifier (LM) usage prior to 2 weeks of recruitment or following plan.
- •Have used systemic/inhaled steroid prior to 2 weeks of recruitment
结局指标
主要结局
Patient Symptom Score
时间窗: 7 weeks (plus or minus 3 days )
次要结局
- Patient Compliance Report(7 weeks (plus or minus 3 days ))
- Investigator Assessment Report(7 weeks (plus or minus 3 days ))
研究者
研究点 (1)
Loading locations...
相似试验
已完成
不适用
Intervention trial of asthmatic cough therapycough variant asthmaJPRN-UMIN000001023Japanese cough variant asthma research society180
Unknown
不适用
Cough Suppressive Therapy in Patients With Chronic CoughChronic CoughNCT05522699Uppsala University100
已完成
不适用
A 3-Month Non-Interventional Study of Asthmatics Treatment With Symbicort® Turbuhaler®AsthmaNCT00532922AstraZeneca310
已完成
不适用
NIS-observe Treatment Efficacy in Maintaining Symptoms Control in Moderate/Severe Asthma With Symbicort SMARTModerate/Severe AsthmaNCT00785733AstraZeneca1,182
尚未招募
Unknown
Validation of new indicators related to treatment decisions for bronchial asthmaBronchial asthmaJPRN-UMIN000053589Yokohama Minami Kyosai Hospital100