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
0.2
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
- 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: