JPRN-UMIN000003492已完成4 期
Efficacy and safety of regular treatment with procaterol and budesonide inhalation suspension for young children with moderate persistent asthma. - Budesonide + Procaterol Inhalation Therapy Study (BUPIT study)
niversity of Toyama, Faculty of Medicine, Department of Pediatrics0 个研究点目标入组 50 人开始时间: 2010年4月14日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 6months-old 至 60months-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1.Patients who have an event listed below within a month a)Respiratory infection disease that required hospitalization b)Administration of systemic corticosteroids 2.Recieving regular use of inhaled corticosteroids or beta 2 agonists in the previous 3 months 3.Patients who have severe chronic diseases 4.Patients who have chronic low airway diseases other than bronchial asthma 5.Any other children considered by the attending physicians as inappropriate for participation in this study
研究者
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