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临床试验/NCT02128529
NCT02128529已完成不适用

A Cross-sectional Observational Study in Pulmonology Departments in Belgium and Luxembourg to Investigate the Epidemiology of Chronic Bronchitis in Patients Suffering From Moderate to Very Severe COPD

AstraZeneca0 个研究点目标入组 976 人开始时间: 2010年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
AstraZeneca
入组人数
976
主要终点
Percentage of Participants with Chronic Bronchitis

研究概览

简要总结

The purpose of this study was to investigate the prevalence of chronic bronchitis in patients suffering from moderate to very severe chronic obstructive pulmonary disease (COPD), and to assess the difference in exacerbation rates in patients suffering from moderate to very severe COPD with chronic bronchitis vs. a population of patients without chronic bronchitis.

详细描述

This was an observational study so participants only took medication that was prescribed by their regular healthcare provider. No additional study medication was administered. This study enrolled patients who were previously diagnosed with moderate to very severe chronic obstructive pulmonary disease (COPD). This study looked at the prevalence of chronic bronchitis in patients suffering from moderate, severe or very severe COPD, and it also compared worsening of COPD in patients with or without chronic bronchitis. This study enrolled 976 patients. This multi-centre trial was conducted in Belgium and Luxembourg. The overall time to participate in this study was at a single, regularly scheduled visit at the pulmonologists office. There were no follow-up assessments for this study.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Written informed consent.
  • Age ≥ 40 years.
  • Forced expiratory volume in one second (FEV1)/Forced vital capacity (FVC) ratio (post-bronchodilator) <70%.
  • FEV1 (post-bronchodilator) < 80% of predicted.

排除标准

  • Moderate and severe exacerbations during the last 4 weeks.
  • Already participated in the study (allowed to participate only once).

结局指标

主要结局

Percentage of Participants with Chronic Bronchitis

时间窗: 2 years prior to the study visit on Day 1

Chronic bronchitis is defined as the presence of cough and sputum production for at least 3 months in each of 2 consecutive years.

Exacerbation Rate

时间窗: 12 Months prior to the study visit

An exacerbation is defined as an event in the natural course of the disease characterised by a change in the patient's baseline dyspnoea, cough, and/or sputum that is beyond normal day-to-day variations, is acute in onset, and may warrant a change in regular medication in a patient with underlying COPD for three or more days. Exacerbation rate is defined as number of exacerbations per year.

次要结局

  • Percentage of Participants with Moderate, Severe or Very Severe COPD(At the study visit (Day 1))
  • Percentage of Participants with Risk Factors(12 months prior to study visit)
  • Changes in Post-bronchodilator forced expiratory volume after 1 second (FEV1)(At the study visit, and 6 months and 12 Months prior to study visit)
  • Percentage of Participants with Other Relevant Diseases(12 months prior to study visit)
  • COPD Treatment(At the study visit (Day 1))
  • Changes in post-bronchodilator ratio of FEV1 to forced vital capacity (FVC)(At the study visit, and 6 months and 12 Months prior to study visit)

研究者

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

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