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临床试验/EUCTR2013-000808-41-HU
EUCTR2013-000808-41-HU进行中(未招募)不适用

Randomized, double-blind, double-dummy, active-controlled, 4 period complete cross-over study to compare the effect on lung function of 6 weeks once daily treatment with orally inhaled tiotropium+olodaterol fixed dose combination delivered by the Respimat® inhaler vs. 6 weeks twice daily treatment with fluticasone propionate+salmeterol fixed dose combination delivered by the Accuhaler® in patients with Chronic Obstructive Pulmonary Disease (COPD) - ENERGITO

Boehringer Ingelheim RCV GmbH&Co KG0 个研究点目标入组 308 人开始时间: 2013年8月13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
308

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

  • 1. Diagnosis of chronic obstructive pulmonary disease
  • 2. Relatively stable airway obstruction with a post-bronchodilator 30% 3. Male or female patients, 40 years of age or older
  • 4. Smoking history of more than 10 pack years
  • 5. Ability to perform technically acceptable pulmonary function tests and maintain records
  • 6. Ability to inhale medication in a competent manner from the RESPIMAT Inhaler, Accuhaler and from a metered dose inhaler (MDI)
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 114
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 114

排除标准

  • 1. Significant disease other than COPD
  • 2. COPD exacerbation that required treatment with antibiotics, systemic steroids (oral or iv) or hospitalization in the last 3 months.
  • 3. Clinically relevant abnormal lab values
  • 4. History of asthma
  • 5. Diagnosis of thyrotoxicosis
  • 6. Diagnosis of paroxysmal tachycardia
  • 7.History of myocardial infarction
  • 8. Unstable or life-threatening cardiac arrhythmia
  • 9. Hospitalization for heart failure within the past year
  • 10. Known active tuberculosis
  • 11. malignancy for which patient has undergone resection, radiation therapy or chemotherapy within last five years
  • 12. History of life-threatening pulmonary obstruction
  • 13.History of cystic fibrosis
  • 14. Clinically evident bronchiectasis
  • 15.History of significant alcohol or drug abuse
  • 16. History of thoracotomy with pulmonary resection
  • 17. oral or patch ß-adrenergics
  • 18. Oral corticosteroid medication within 6 weeks prior to Visit 1
  • 19. Regular use daytime oxygen therapy for more than one hour per day
  • 20. Pulmonary rehabilitation program in the six weeks prior to the screening visit
  • 21. Investigational drug within one month or six half lives (whichever is greater) prior to screening visit
  • 22. Known hypersensitivity to ß-adrenergic drugs, BAC, EDTA
  • 23. Pregnant or nursing women

研究者

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已完成
3 期
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