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NCT00470327 Clinical Trial

A Study of the Natural Progression of Interstitial Lung Disease (ILD)

Idiopathic Pulmonary Fibrosis Clinical Trial

Official title:
A Study of the Natural Progression of Interstitial Lung Disease (ILD)

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00470327
Other study ID # 14163A
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 2005
Est. completion date December 2025

Study information
Verified date November 2023
Source University of Chicago
Contact Spring Maleckar
Phone 773-834-4053
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

We propose to acquire data and blood samples on all patients being cared for by the Interstitial Lung Disease (ILD) program. Additionally, we will collect data and blood samples from a control group for comparator purposes. In doing so, we will be able to describe the "phenotypic" expression of these diseases.

Recruitment information / eligibility
Status Recruiting
Enrollment 4000
Est. completion date December 2025
Est. primary completion date December 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Interstitial lung disease Exclusion Criteria: - Does not have Interstitial lung disease

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States University of Chicago Chicago Illinois

Sponsors (2)
Lead Sponsor Collaborator
University of Chicago Idiopathic Pulmonary Fibrosis Clinical Research Network

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Natural history of course of disease in patients with Interstitial lung disease (ILD) We assess mortality roughly yearly but duration is unlimited Yearly
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