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Establishment of a Sophisticated Cohort on Early Chronic Obstructive Pulmonary Disease

Establishment of a Sophisticated Cohort on Early Chronic Obstructive Pulmonary Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126359
Enrollment
Unknown
Registered
2026-06-08
Start date
2026-06-08
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

Early chronic obstructive pulmonary disease

Interventions

Observation group 1 (Male participants aged = 50 years):N/A
Observation group 3(Female participants aged >= 50 years):N/A

Sponsors

China-Japan Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Age 18-60 years; 2.Both genders (male or female); 3.Post-bronchodilator lung function FEV1/FVC = 0.70 but FEV1 and/or FVC < 80% of predicted value, or FEV1/FVC = lower limit of normal (LLN) but FEV1 < LLN; 4.Exposure to modifiable risk factors (such as direct smoking, secondhand smoke, biomass fuel, occupational dust or chemical substances, outdoor air pollution, etc.) and/or potential treatable traits (such as chronic cough, chronic cough with phlegm, chest tightness, significant shortness of breath or difficulty with breathing after activities, frequently suffered from respiratory infection, comorbid with bronchial asthma, etc.); 5.Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Self-reported a history of interstitial lung disease, bronchiectasis, tuberculosis-related lung damage, lung cancer, pleural effusion, or other diseases that caused restrictive ventilatory function, or underwent a lung resection surgery or lung transplantation; 2.Suffering from other major physical and/or psychological illnesses, unable to undergo questionnaire survey and physical examination; 3.Having active pulmonary tuberculosis or other infectious diseases; 4.Had a lower respiratory tract infection in the past four weeks; 5.Ever used or currently using short-acting and/or long-acting bronchodilators to treat chronic airway diseases (including but not limited to COPD, bronchial asthma, chronic bronchitis, bronchiectasis, etc.); 6.Pregnant women, or women within the first year after giving birth; 7.Currently participating in medical research involving drug and/or non-drug interventions.

Design outcomes

Primary

MeasureTime frame
The change of post-bronchodilator FEV1, the change of CAT score, and/or the number of acute exacerbation events of respiratory symptoms at one-year assessment;

Secondary

MeasureTime frame
Post-bronchodilator FEV1/FVC < LLN (i.e. airflow limitation) at one-year assessment;Post-bronchodilator FEV1/FVC < 0.70 (i.e. airflow limitation) at one-year assessment;The number of acute exacerbation events of respiratory symptoms at one-year assessment;The change of post-bronchodilator FEV1 at one-year assessment;The average rate of decline with post-bronchodilator FEV1 at one-year assessment;The change of CAT score at one-year assessment;

Countries

China

Contacts

Public ContactLei Jieping

China-Japan Friendship Hospital

jiepinglei@126.com+86 10 84206408

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026