NL-OMON39121已完成不适用
Assessment of Comorbidities in COPD in European Symptomatic Subjects from primary care. - ACCESS
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 480
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •1. Males/females >= 40 years of age.
- •2. COPD (all GOLD-stages) diagnosed >= 12 months ago.
- •3. FEV1/FVC (tiffeneau-index) after use of bronchodilator < 0.70.
- •4. Smoking history of >= 10 packyears
- •5. Singed informed consent form.
排除标准
- •1.In the opinion of the investigator, there is a current primary diagnosis of asthma (patients with a primary diagnosis of COPD but who also have asthma may be included)
- •2.A diagnosis of fibrosis or asbestosis
- •3.Diagnosis of cancer - includes current and within the last 5 years (patients in remission for >= 5 years may be included). Patients diagnosed with cancer during the study will be withdrawn
- •4.Diagnosis of clinically significant bronchiectasis
- •5.Subjects who are concurrently participating in any clinical study or who have received any investigational drugs within 4 weeks of Visit 1, or who will start any during the study period.
- •6.Unable to or unwilling to conform with the study requirements including completion of the health status questionnaires
- •7.Females who are pregnant or lactating.
研究者
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