EUCTR2009-015876-86-GB进行中(未招募)不适用
An investigation into the mechanisms of action of a combined long acting beta agonist/inhaled corticosteroid (Seretide 500 accuhaler) on the bacterial colonisation, immunology and inflammation of patients with Chronic Obstructive Pulmonary Disease (COPD) - An investigation of the mechanism of action of Seretide in COPD
Southampton University Hospitals0 个研究点开始时间: 2010年3月29日最近更新:
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试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
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
- •COPD will be defined as forced expiratory volume in one second (FEV1) of <80% predicted for age and height, and salbutamol reversibility of <400 ml with airflow obstruction evidenced by a ratio of FEV1 to forced vital capacity (FVC) of <70%. A minimum of a 10 pack year history in all groups. Healthy smokers will be subjects who have smoked a minimum of 10 pack years but have normal lung function, they will be matched in all other criteria to the COPD patients. Mild, moderate and severe patients will be defined by FEV1. Mild >50-80% Moderate >30%-50% Severe <30% The COPD patients are to have never used components present in the Seretide (Salmeterol and flixotide)
- •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 0
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 0
排除标准
- •Patients with a history of asthma, bronchiectasis, carcinoma of the bronchus, or other significant respiratory disease will be excluded. A comprehensive history, chest x-ray and reversibility studies performed on this cohort will be used to identify those with other lung pathology. Patients will also be excluded if they have exacerbated during the last 6 weeks. Patients will also be excluded if they have been prescribed inhaled corticosteroids for the treatment of their condition.
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