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Idiopathic Pulmonary Fibrosis and Serum Bank — FPI  

Idiopathic Pulmonary Fibrosis Clinical Trial

Official title:
Idiopathic Pulmonary Fibrosis and Serum Bank

Clinical Trial Summary

Idiopathic pulmonary fibrosis (IPF) is the most common form of chronic idiopathic diffuse interstitial lung disease (DILD) in adults. It is a fibroproliferative, irreversible disease of unknown cause, usually progressive, occurring mainly from the age of 60 and limited to the lungs. IPF is a serious disease with a median survival rate at diagnosis of 3 years. The aim of the study is to set up a biocollection of serum from patients in a context of idiopathic DILD and a possible or confirmed diagnosis of common interstitial lung disease by chest CT. Patients will be recruited at the consultations of the Rennes Rare Lung Disease Competence Centre. These will be patients in stable condition or in acute exacerbation of IPF.

Clinical Trial Description

This study will initially focus on circulating serum CD163 markers, but a broader proteomics approach could be considered in a second phase to look for other markers of lung diseases. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04016168
Study type Observational
Source Rennes University Hospital
Contact
Status Completed
Phase
Start date October 22, 2014
Completion date December 28, 2022
View Details
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