JPRN-UMIN000005063已完成未知
Study of step down from high dose of salmeterol/fluticasone propionate combination(SFC) with tiotropium to middle dose of SFC + ciclesonide(CIC) with tiotropium in well controlled asthmatic patients with COPD - Study of step down from high dose SFC with tiotropium to middle dose SFC + CIC with tiotropium in well controlled asthmatic patients with COPD
Department of Respiratory Medicine, Graduate school of Medicine, Osaka City University0 个研究点目标入组 50 人开始时间: 2011年2月10日最近更新:
适应症
试验速览
- 阶段
- 未知
- 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
- 40years-old 至 ot applicable(—)
- 性别
- All
入选标准
- 未提供
排除标准
- •1)asthma control test score < 20 2)infection with bacteria or fungus 3)pregnancy 4)current smoker 5)investigator decision
研究者
相似试验
已完成
不适用
Treatment effect of switching from salmeterol/fluticasone to formoterol/budesonide combinations in patients with asthmaAsthmaJPRN-UMIN000009619Hamamatsu University School of Medicine60
已完成
4 期
Study to examine the effects of Salmeterol/fluticasone propionate combination(SFC) in patients with cough variant asthma(CVA)Cough variant asthmaJPRN-UMIN000002390Kyoto University Graduate School of Medicine60
已完成
不适用
Assessments of the effect of Salmeterol and Fluticasone Propionate (SFC250) on the patients with chronic obstructive pulmonary disease by Impulse OscillometryChronic Obstructive Pulmonary DiseaseJPRN-UMIN000004196St. Marianna University School of Medicine, Division of Respiratory and Infectious Diseases200
已完成
不适用
Comparison of Clinical Effects of Salmeterol/Fluticasone Propionate Combination Products Delivered via Metered-Dose Inhaler with Dry Powder Inhaler in Patients with Moderate AsthmaBronchial asthmaJPRN-UMIN000009990ational Center for Global Health and Medicine40
进行中(未招募)
不适用
Efficacy and safety of Salmeterol/Fluticasone DPI HEXAL versus Seretide™ Accuhaler™ in adolescent and adult patients with moderate-to-severe persistent asthma: A 12-week, multicenter, randomized, double-blind, double-dummy, parallel group studyEUCTR2007-005620-32-LTHEXAL AG472
