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RECRUITINGOBSERVATIONAL

Creation of a Biospecimen Repository From Patients With Interstitial Lung Diseases (ILD)

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

To develop a repository of blood samples from patients with ILD to support future studies into the development of such biomarkers. Patients with pneumonia and healthy patients will also be recruited as a control group.

Who May Be Eligible (Plain English)

Who May Qualify: - Patients with a diagnosis of ILD or any fibrotic disease of the lung or a diagnosis of pneumonia - Patients willing to provide written willing to sign a consent form Who Should NOT Join This Trial: - Unwillingness/unable to give blood samples Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Patients with a diagnosis of ILD or any fibrotic disease of the lung or a diagnosis of pneumonia * Patients willing to provide written informed consent Exclusion Criteria: * Unwillingness/unable to give blood samples

Treatments Being Tested

OTHER

ILD

100 cc of blood collected from a total of 250 ILD patients. This includes IPF (n=100), fibrotic NSIP (n=50), chronic hypersensitivity pneumonia (n=20), sarcoidosis(n=50), progressive rheumatoid lung disease (n=10) and scleroderma lung disease (n=20)), 10 patients with other fibrosing disease (fibrosing mediastinitis), and 50 patients with lymphangioleiomyomatosis

OTHER

Healthy

100 cc of blood collected from a total of 25 healthy volunteers in order to compare with the ILD participants.

OTHER

Pneumonia

100 cc of blood collected from a total of 100 participants with a diagnosis of pneumonia in order to compare with the ILD participants.

Locations (1)

Mayo Clinic
Rochester, Minnesota, United States