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临床试验/ACTRN12615000336583
ACTRN12615000336583招募中未知

The effects of administration of dual long-acting bronchodilators (beta-agonists and muscarinic-antagonists), compared to mono therapy, on complex lung mechanics in patients with mild to moderate chronic obstructive pulmonary disease

Woolcock Institute of Medical Research0 个研究点目标入组 25 人开始时间: 2015年4月14日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
25

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
40 Years 至 80 Years(—)
性别
All

入选标准

  • Adults with physician-diagnosed mild-moderate chronic obstructive pulmonary disease, with a history of current or past smoking (total exposure > 10 pack years)

排除标准

  • * Use of glycopyrronium, indacaterol, salmeterol or any other LAMA or LABA within the previous 4 weeks (unless able to undergo a 2 week washout period)
  • * Documented hypersensitivity to, or intolerance of, beta-agonists or anti-cholinergic therapies
  • * Significant respiratory infection or documented exacerbation of COPD within the previous 6 weeks
  • * Other active or chronic respiratory pathologies (for example, interstitial lung disease, asthma, chest wall pathology causing ventilatory restriction)
  • * Past history of lung surgery (including lobectomy or pneumonectomy, but not lung biopsy) or thoracic radiation therapy (excluding isolated mediastinal radiation therapy with no evidence of subsequent pulmonary fibrosis)
  • * Any major comorbidities deemed to impact on respiratory physiology or symptoms, including severe on uncontrolled heart failure, morbid obesity, muscular or neurological disorders causing respiratory muscle weakness or dysfunctional swallowing
  • * History of severe renal or hepatic impairment
  • * Unable to perform lung function testing at the enrollment visit
  • * Dependence on domiciliary supplemental oxygen, unable to go without for at least 1 hour
  • * Women who are breast feeding, pregnant, or unwilling to avoid pregnancy during the study period
  • * Unable to provide informed consent
  • * Current enrolment in other trials

研究者

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