NL-OMON51461已完成不适用
A multi-center, real-world exploratory cohort study to evaluate cough frequency, severity, and impact on quality of life in patients with non-idiopathic pulmonary fibrosis interstitial lung disease - Evaluating cough and impact on quality of life in pulmonary fibrosis
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 10
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
- •- Provision of signed informed consent in writing prior to study data collection
- •- Subject aged 18 years or over
- •- Subject diagnosed with non-IPF fibrosing ILD
排除标准
- •- Cough due to etiology other than ILD (e.g., allergic rhinitis,
- •Gastroesophageal Reflux Disease (GERD))
- •- Other respiratory disorders including, but not limited to, a current
- •diagnosis of any obstructive disease including chronic obstructive pulmonary
- •disease (COPD) and asthma, active tuberculosis, lung cancer in treatment or in
- •medical history, sleep apnea, known alpha-1 antitrypsin deficiency, cor
- •pulmonale, clinically significant pulmonary hypertension, clinically
- •significant bronchiectasis, or other active pulmonary diseases
- •- Respiratory infection or use of antibiotics for respiratory cause within 4
- •weeks prior to study entry
- •- Initiation or change in dose or type of anti-tussive medication,
- •angiotensin-converting enzyme (ACE) inhibitors, or corticosteroids in the 4
- •weeks prior to study entry
- •- Subject with airflow obstruction (forced expiratory volume in one second
- •(FEV1)/FVC<0.7) or known significant spirometry response to bronchodilator
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