Inflammation in Interstitial Lung Disease/Idiopathic Pulmonary Fibrosis
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Lung Disease, Interstitial
- Sponsor
- Ohio State University
- Enrollment
- 13
- Locations
- 1
- Primary Endpoint
- Framework
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
To establish a registry of patients for future studies of Inflammation in Interstitial Lung Disease/Idiopathic Pulmonary Fibrosis.
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.
Investigators
Eligibility Criteria
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
Outcomes
Primary Outcomes
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