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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorMayo Clinic

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Disqualifiers

Unwillingness/unable to give blood samples

Trial population

Patients with a diagnosis of ILD or any fibrotic disease of the lung. A diagnosis of pneumonia and healthy volunteers will also be included as a control group.

Trial design

Design model

Other

Time perspective

Retrospective

Treatments tested in this trial

  • ILD

    Other intervention

    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

  • Healthy

    Other intervention

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

  • Pneumonia

    Other intervention

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

Treatment groups

635 Participants
are divided into 3 treatment groups
Group A: ILD1 intervention
Group B: Healthy1 intervention
Group C: Pneumonia1 intervention

Trial outcomes

Primary outcomes

1

Future Disease Management

Reliable biomarkers to help guide treatment in ILD would be a major step forward in the management of this disease.

Time frame
1 visit

Secondary outcomes

Other outcomes

Sponsors and contacts

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