Idiopathic Pulmonary Fibrosis Registry for Future Studies

Sponsor
Ohio State University (Other)
Overall Status
Completed
CT.gov ID
NCT00815711
Collaborator
(none)
13
1
78.3
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Study Details

Study Description

Brief Summary

To establish a registry of patients for future studies of Inflammation in Interstitial Lung Disease/Idiopathic Pulmonary Fibrosis.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    To establish a framework in which biologic samples and physiologic measures from patients with IPF can be longitudinally collected and evaluated. Having a bank of samples that are correlated with physiologic measures that follow patients through their course will allow the following proposed studies as well as future investigations to be efficiently carried out.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    13 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Inflammation in Interstitial Lung Disease/Idiopathic Pulmonary Fibrosis
    Actual Study Start Date :
    Dec 1, 2008
    Actual Primary Completion Date :
    Jun 10, 2015
    Actual Study Completion Date :
    Jun 10, 2015

    Outcome Measures

    Primary Outcome Measures

    1. Framework [7 + years]

      To establish a framework in which biologic samples and physiologic measures from patients with IPF can be longitudinally collected and evaluated

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • any patient referred to the Interstitial Lund Disease clinic who is undergoing evaluation and or treatment for a new diagnosis of ILD. This can include patients referred for presumed pulmonary fibrosis/interstitial pneumonitis (IPF, UIP, NSIP), sarcoidosis, hypersensitivity pneumonitis, cryptogenic organising pneumonia, drug-induced, or other idiopathic ILDs.
    Exclusion Criteria:
    • pregnancy

    • inability to follow study requirements

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The Ohio State University Columbus Ohio United States 43210

    Sponsors and Collaborators

    • Ohio State University

    Investigators

    • Principal Investigator: Clay B Marsh, MD, Ohio State University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ohio State University
    ClinicalTrials.gov Identifier:
    NCT00815711
    Other Study ID Numbers:
    • 2007H0002
    First Posted:
    Dec 30, 2008
    Last Update Posted:
    Nov 8, 2021
    Last Verified:
    Nov 1, 2021
    Keywords provided by Ohio State University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 8, 2021