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Idiopathic Pulmonary Fibrosis Registry for Future Studies

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ClinicalTrials.gov Identifier: NCT00815711
Recruitment Status : Unknown
Verified August 2014 by Clay Marsh MD, Ohio State University.
Recruitment status was:  Recruiting
First Posted : December 30, 2008
Last Update Posted : August 22, 2014
Sponsor:
Information provided by (Responsible Party):
Clay Marsh MD, Ohio State University

December 29, 2008
December 30, 2008
August 22, 2014
December 2008
January 2015   (Final data collection date for primary outcome measure)
Framework [ Time Frame: 7 + years ]
To establish a framework in which biologic samples and physiologic measures from patients with IPF can be longitudinally collected and evaluated
Not Provided
Complete list of historical versions of study NCT00815711 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Idiopathic Pulmonary Fibrosis Registry for Future Studies
Inflammation in Interstitial Lung Disease/Idiopathic Pulmonary Fibrosis
To establish a registry of patients for future studies of Inflammation in Interstitial Lung Disease/Idiopathic Pulmonary Fibrosis.
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.
Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Retention:   Samples With DNA
Description:
blood serum BAL fluid lung biopsy
Non-Probability Sample
primary care clinic
  • Lung Disease, Interstitial
  • Idiopathic Pulmonary Fibrosis
Not Provided
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Unknown status
84
Same as current
January 2015
January 2015   (Final data collection date for primary outcome measure)

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
Sexes Eligible for Study: All
18 Years and older   (Adult, Older Adult)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00815711
2007H0002
No
Not Provided
Not Provided
Clay Marsh MD, Ohio State University
Clay Marsh MD
Not Provided
Principal Investigator: Clay B Marsh, MD Ohio State University
Ohio State University
August 2014