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Clinical Trials in China / NCT05895409
Recruiting Observational

A Multicenter Prospective Study of Risk Factors in Progressive Pulmonary Fibrosis

NCT05895409 · tracked via the Priya Life Science China tracker
Sponsor
Qianfoshan Hospital
Phase
Observational
Started
2023-07-27
Last updated
2023-11-18

Condition(s) studied

Interstitial Lung Disease

Study summary

The goal of this observational study is to learn about risk of progressive pulmonary fibrosis (PPF). The main questions it aims to answer are:

* Risk factors of PPF
* Prevalence of PPF
* Mortality of PPF

Patients with interstitial lung disease (ILD) of known or unknown etiology other than IPF who has radiological evidence of pulmonary fibrosis will enroll in this study.

* All participants will have baseline investigations at the first visit having provided informed consent.
* At the first visit, baseline characteristics will be collected including demographics, medical history, smoking history, complications and medication use. 50 mL of blood will be obtained. High resolution computed tomography (HRCT), full lung function tests and a 6 min walk test will be performed.
* Further visits at 6 months and 12 months will include further 50 mL blood sampling. HRCT, full lung function tests and a 6 min walk test will be repeated.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * 18-80 years old * Agree and sign the informed consent form * Interstitial lung disease patients with imaging features of pulmonary fibrosis Exclusion Criteria: * Patients with idiopathic pulmonary fibrosis (IPF) * Pregnant or lactating women * mental illness or cognitive impairment * participating in other clinical studies * Unable to sign informed consent form

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The First Affiliated Hospital of Shandong First Medical University Jinan Shandong Recruiting

More Qianfoshan Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05895409 on ClinicalTrials.gov ↗ ← All trials in China