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
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
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