- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00470327
A Study of the Natural Progression of Interstitial Lung Disease (ILD)
November 29, 2023 updated by: University of Chicago
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.
Study Overview
Status
Recruiting
Study Type
Observational
Enrollment (Estimated)
4000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Spring Maleckar
- Phone Number: 773-834-4053
Study Locations
-
-
Illinois
-
Chicago, Illinois, United States, 60637
- Recruiting
- University of Chicago
-
Contact:
- Mary E Strek, MD
- Phone Number: 773-702-3609
- Email: mstrek@medicine.bsd.uchicago.edu
-
Principal Investigator:
- Mary E Strek, MD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Subjects cared for in the ILD (Interstitial Lung Disease)clinic
Description
Inclusion Criteria:
- Interstitial lung disease
Exclusion Criteria:
- Does not have Interstitial lung disease
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Natural history of course of disease in patients with Interstitial lung disease (ILD)
Time Frame: Yearly
|
We assess mortality roughly yearly but duration is unlimited
|
Yearly
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Mary E Strek, MD, University of Chicago
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 1, 2005
Primary Completion (Estimated)
December 1, 2025
Study Completion (Estimated)
December 1, 2025
Study Registration Dates
First Submitted
May 3, 2007
First Submitted That Met QC Criteria
May 4, 2007
First Posted (Estimated)
May 7, 2007
Study Record Updates
Last Update Posted (Actual)
November 30, 2023
Last Update Submitted That Met QC Criteria
November 29, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Pathologic Processes
- Respiratory Tract Diseases
- Immune System Diseases
- Lymphoproliferative Disorders
- Lymphatic Diseases
- Hypersensitivity
- Hypersensitivity, Delayed
- Fibrosis
- Lung Diseases
- Pulmonary Fibrosis
- Idiopathic Pulmonary Fibrosis
- Connective Tissue Diseases
- Lung Diseases, Interstitial
- Sarcoidosis
Other Study ID Numbers
- 14163A
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
We will share coded data with no PHI
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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