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Prognostic prediction of IPF patients based on CDO score

Prognostic prediction of IPF patients based on CDO score

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500098698
Enrollment
Unknown
Registered
2025-03-12
Start date
2025-04-01
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

idiopathic pulmonary fibrosis

Interventions

IPF patient group:None
Validation group:None

Sponsors

Shanghai Pulmonary Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.>=18 years old, male or female; 2.The condition is stable according to the diagnostic criteria of different types of interstitial lung diseases and the diagnosis is determined by MDT discussion Patients with IPF. No acute exacerbation was determined by the investigators; 3.Regardless of whether the patient received antifibrotic therapy or other treatments; 4.Participants who are willing to participate in the study and sign the informed consent, have the ability of autonomous behavior, have good compliance, and are willing to follow the program Ask for tests and regular follow-up;

Exclusion criteria

Exclusion criteria: 1.Diagnosed by clinical doctors with diseases as follows: pulmonary sarcoidosis, lung cancer with ILD at enrollment, cryptogenic organizing pneumonia or radiation induced lung injury, chronic obstructive pulmonary disease (copd), bronchial asthma, infectious lung disease; 2.Patients with other clinically significant abnormalities in the lungs that the investigators determined might affect the study results (e.g., pulmonary embolism, pneumothorax, etc.); 3.Significant extrapulmonary physical or pathological limitations (e.g., chest wall malformations, massive pleural effusion, muscle weakness, diaphragmatic paralysis, etc.); 4.Patients with significant systemic and other diseases that the investigator determines may have an impact on the results of the study (such as severe neurological or cardiovascular diseases); 5.Patients with difficulty in follow-up or who are determined by the researchers to be unable to complete the relevant study (such as pregnant women);

Design outcomes

Primary

MeasureTime frame
1-year IPF all-cause mortality;

Secondary

MeasureTime frame
2-year IPF all-cause mortality;3-year IPF all-cause mortality;First acute exacerbation of IPF;IPF-related event mortality rate;

Countries

China

Contacts

Public ContactQian Yao

Shanghai Pulmonary Hospital

qianyao@tongji.edu.cn+86 139 1772 1342

Outcome results

None listed

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