Viewing Study NCT04016168


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Ignite Modification Date: 2025-12-24 @ 5:35 PM
Study NCT ID: NCT04016168
Status: COMPLETED
Last Update Posted: 2023-11-28
First Post: 2019-07-08
Is Possible Gene Therapy: False
Has Adverse Events: False

Brief Title: Idiopathic Pulmonary Fibrosis and Serum Bank
Sponsor: Rennes University Hospital
Organization:

Study Overview

Official Title: Idiopathic Pulmonary Fibrosis and Serum Bank
Status: COMPLETED
Status Verified Date: 2023-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: FPI
Brief 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.
Detailed 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 Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
2014-A00268-39 OTHER Id-RCB View