Lung Diseases, Interstitial Clinical Trial
Official title:
Non-interventional Study Describing Epidemiology, Clinical Characteristics, Prognosis and Healthcare Costs of PF-ILD and SSc-ILD Patients in France, 2010-2017
Interstitial lung diseases (ILDs) are a heterogeneous group of disorders, which encompass a
wide range of conditions. In some patients with fibrosing ILDs, a progressive phenotype
similar to that observed in idiopathic pulmonary fibrosis (IPF) may develop during the course
of the disease (PF-ILD), including patients with systemic sclerosis (SSc)-related ILD.
The aim of the study is to estimate the incidence and prevalence and to describe the
characteristics of patients diagnosed with non-IPF PF-ILD and SSc-ILD, to describe the
natural course of disease, and to explore the correlation between mortality and Forced Vital
Capacity (FVC) of the patients with non-IPF PF-ILD.
This study will be based on two data sources: the French national medico administrative
database (SNDS) and the ILD cohort from the National French center for rare pulmonary
diseases in Lyon, France.
n/a
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