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临床试验/EUCTR2011-003732-31-NL
EUCTR2011-003732-31-NL进行中(未招募)不适用

A randomized, double-blind, parallel-group, 26-week study comparing the efficacy and safety of indacaterol (Onbrez® Breezhaler® 150 µg o.d.) with salmeterol/fluticasone propionate (Seretide® Accuhaler® 50 µg/500 µg b.i.d.) in patients with moderate chronic obstructive pulmonary disease.

ovartis Pharma Services AG0 个研究点目标入组 600 人开始时间: 2012年1月4日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
600

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Patients with moderate COPD (Stage II)
  • - Able to perform spirometry assessments
  • - Current or ex-smokers
  • - On treatment with the fixed-dose combination of salmeterol 50 µg /fluticasone propionate 500 µg MDDPI b.i.d. for the treatment of COPD for =3 months directly
  • Other protocol-defined inclusion/exclusion criteria may apply.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 450
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 150

排除标准

  • - Having had a COPD exacerbation that required treatment with antibiotics and/or oral corticosteroids and/or hospitalization in the past year.
  • - A history of, or current ECG abnormality.
  • Other protocol-defined inclusion/exclusion criteria may apply.

研究者

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