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A Prospective, Multi-Center Registry Study of Progressive Pulmonary Fibrosis (PPF) in China (PROFINA)

A Prospective, Multi-Center Registry Study of Progressive Pulmonary Fibrosis (PPF) in China (PROFINA)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500103174
Enrollment
Unknown
Registered
2025-05-26
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-06-02

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

Conditions

Progress Pulmonary Fibrosis

Interventions

Observation group:NA

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosis of PPF within the past year, according to the 2022 ATS/ERS/JRS/ALAT guidelines; 2. Patients who are willing to participate in the study and have signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients diagnosed with IPF. 2.Patients without baseline chest HRCT. 3. Patients who refuse to sign the informed consent form. 4. Patients participating in other clinical trials for medications. (Patients who have completed other trials or are in an unblinded phase after a washout period of 2 weeks are eligible for enrollment.);

Design outcomes

Primary

MeasureTime frame
Forced Vital Capacity, FVC;

Secondary

MeasureTime frame
Connective Tissue Disease Associated Interstitial Lung Disease, CTD-ILD;Hypersensitivity Pneumonitis, HP;Idiopathic Non-Specific Interstitial Pneumonitis, iNSIP;

Countries

China

Contacts

Public ContactXu Zuojun

Peking Union Medical College Hospital

xuzj@hotmail.com+86 136 7134 5136

Outcome results

None listed

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