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Analysis of risk factors for acute exacerbation of chronic obstructive pulmonary disease: a case-control study

Analysis of risk factors for acute exacerbation of chronic obstructive pulmonary disease: a case-control study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400087391
Enrollment
Unknown
Registered
2024-07-26
Start date
2024-08-01
Completion date
Unknown
Last updated
2024-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic obstructive pulmonary disease

Interventions

Stable COPD subjects:None
AECOPD subjects:None

Sponsors

Zhujiang Hospital, Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: Stable COPD subjects: (1) age = 40 years; (2) persistent respiratory symptoms, including recurrent cough, sputum and progressive dyspnea, with no significant aggravation of the above symptoms in the past 14 days; (3) the presence of irreversible airflow limitation (FEV1/FVC <70% after the inhalation of bronchodilators), with an improvement in the rate of FEV1 <12% and the improvement in the amount of FEV1 <200 ml. AECOPD subjects: (1) age = 40 years; (2) persistent respiratory symptoms, including recurrent cough, sputum and progressive dyspnea, in the past 14 days the above symptoms suddenly worsened, exceeding the range of daily variability, and self-adjustment of drugs can not be improved; (3) the existence of irreversible airflow limitation (after inhalation of bronchodilators, FEV1/FVC <70%), the rate of improvement of FEV1 <12% and the amount of improvement <200ml. FEV1/FVC <70% after inhalation of bronchodilators, FEV1 improvement rate <12% and improvement volume <200ml.

Exclusion criteria

Exclusion criteria: Stable COPD subjects: ? Combined with other lung diseases affecting respiratory symptoms and lung structure, such as bronchiectasis, diffuse panuveitis, pneumonia, active tuberculosis, lung cancer, pulmonary atelectasis, post-pneumonectomy, pulmonary embolism, interstitial lung disease, etc.; ? Combined with pleural and thoracic diseases, such as large amount of pleural effusion, pneumothorax, obvious occupation of the pleura, and thoracic deformities; ? Combined with extrapulmonary diseases affecting respiratory symptoms, such as cardiogenic pulmonary edema, severe anemia, malaise, etc.; ? Combined with incomplete clinical data of lung function, etc. symptoms of extrapulmonary diseases, such as cardiogenic pulmonary edema, severe anemia, malignant fluid, etc.; ? incomplete clinical data such as lung function. AECOPD subjects: ? Combined with other lung diseases affecting respiratory symptoms and lung structure, such as bronchiectasis, diffuse panbronchiolitis, pneumonia, active tuberculosis, lung cancer, pulmonary atelectasis, post-pneumonectomy, pulmonary embolism, interstitial lung disease, etc.; (2) Combined with pleural and thoracic diseases, such as large amount of pleural effusion, pneumothorax, obvious occupation of the pleura, and thoracic deformities; (3) Combined with extrapulmonary diseases affecting respiratory symptoms, such as cardiogenic pulmonary edema, severe anemia, malaise, etc.; (4) incomplete clinical data on pulmonary function. (iii) Combination of extrapulmonary diseases affecting respiratory symptoms, such as cardiogenic pulmonary edema, severe anemia, malignant fluid, etc.; (iv) Incomplete clinical data on pulmonary function.

Design outcomes

Primary

MeasureTime frame
Forced Expiratory Volume in one second;

Countries

China

Contacts

Public ContactChen Xin

Zhujiang Hospital, Southern Medical University

chen_xin1020@163.com+86 139 0220 5193

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026