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Evaluation of Treatment Patterns in Clinical Practice for Adults with Progressive Pulmonary Fibrosis (PPF) Previously Treated with Antifibrotic Therapy

Evaluation of Treatment Patterns in Clinical Practice for Adults with Progressive Pulmonary Fibrosis (PPF) Previously Treated with Antifibrotic Therapy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600128805
Enrollment
Unknown
Registered
2026-07-27
Start date
2025-03-27
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Progressive Pulmonary Fibrosis

Interventions

Observation Group:None

Sponsors

Shanghai Pulmonary Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=18 years, regardless of gender; 2. Have a diagnosis of PPF after March 1, 2023 (with a combination of high-resolution CT (HRCT), pulmonary function test, etc.) and at least 1 follow-up visit within 1 year of diagnosis; 3. Have a clear medical record and diagnosis based on at least one chest CT within 6-12 months of diagnosis, and based on the last CT in a 1-year period; 4. Received at least 1 antifibrotic therapy.

Exclusion criteria

Exclusion criteria: 1. Patients enrolled in another unblinded interventional lung disease-related study prior to enrollment; 2. Patients with serious comorbidities or other conditions (e.g., unrecovered major surgery or trauma, etc.) that, in the judgment of the investigator, may affect the conduct of the study or interpretation of the results; 3. Serious heart disease, such as New York Heart Association (NYHA) Class II-IV heart failure, unstable angina, myocardial infarction, or severe arrhythmia; 4. Uncontrolled hypertension (systolic blood pressure > 160 mmHg and/or diastolic blood pressure > 100 mmHg); 5. Active infections such as human immunodeficiency virus (HIV) infection, active tuberculosis or other infectious diseases requiring systemic anti-infective therapy; 6. Severe liver disease or kidney disease, such as cirrhosis, liver failure, severe hepatitis, chronic kidney disease requiring dialysis, or acute renal failure; 7. Other conditions deemed inappropriate for inclusion by the investigator.

Design outcomes

Primary

MeasureTime frame
Pulmonary Function Indicators(FVC?FVC%?FEV1,etc);

Secondary

MeasureTime frame
Diffusing Capacity of the Lungs for Carbon Monoxide (DLCO);

Countries

China

Contacts

Public ContactBai Jiuwu

Shanghai Pulmonary Hospital

yv59@163.com+86 21 65115006

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026