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Analysis of risk for predicting lung function decline in patients with pre-COPD base on radiomics of Artificial intelligence

Analysis of risk for predicting lung function decline in patients with pre-COPD base on radiomics of Artificial intelligence

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500098752
Enrollment
Unknown
Registered
2025-03-13
Start date
2025-03-24
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

Respiratory Disease

Interventions

Pre-COPD group :NA
Early stage COPD group :NA

Sponsors

Tianjin Chest Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age: 35-75 years old. 2. Gender: male or female. 3. Lung function after inhalation of bronchodilators is consistent with: FEV1/FVC =80%. 4. The patient is willing and able to complete the entire trial process and sign the informed consent form and other relevant documents.

Exclusion criteria

Exclusion criteria: 1. Have diseases that may cause abnormal lung function in the opinion of the clinician, such as lung cancer, bronchiectasis, interstitial lung disease, history of previous chest surgery, etc. 2. Body mass index (BMI) > 35 kg/m^2. 3. Suffering from mental illness or cognitive dysfunction. 4. Pregnant or lactating women. 5. Participating in other interventional clinical studies. 6. Have had a heart attack (angina, myocardial infarction, malignant arrhythmia, etc.) in the past 3 months. 7. Hospitalization for heart disease within the past 1 month. 8. Being treated with anti-tuberculosis drugs or active tuberculosis. 9. Newly identified and treated malignancies. 10. Patients with pulmonary function that other investigators believe are not suitable for undergoing pulmonary function. 11. Inability to provide written informed consent.

Design outcomes

Primary

MeasureTime frame
PRMEmphV(cc);

Secondary

MeasureTime frame
PRMfSADV (cc);Vessel Area(mm2);Total Surface LAA(mm2));

Countries

China

Contacts

Public ContactLi Yi

Tianjin Chest Hospital

13752690754@163.com+86 137 5269 0754

Outcome results

None listed

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