Last updated on November 2019

Idiopathic Pulmonary Fibrosis and Interstitial Lung Disease Prospective Outcomes Registry


Brief description of study

This registry will collect data on the strategies used to achieve a diagnosis of Idiopathic Pulmonary Fibrosis (IPF) and Chronic Fibrosing Interstitial Lung Disease with Progressive Phenotype (ILD) and the treatment and management efforts applied throughout study follow-up, clinical outcome events and patient reported outcome data. Blood samples will be collected periodically throughout the study for use in future research efforts. For participants with non-IPF, chronic fibrosing ILD with progressive phenotype, HRCT images will be collected throughout the study for use in future research efforts.

Clinical Study Identifier: NCT01915511

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University from Virginia

Baltimore, MD United States
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