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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03478826
Enrollment
635
Registered
2018-03-27
Start date
2018-08-01
Completion date
2028-01-01
Last updated
2026-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Interstitial Lung Disease

Keywords

ILD

Brief summary

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.

Detailed description

The proposed biospecimen repository would be derived from patients diagnosed with ILD. This is to include 500 patients in the repository, with each patient contributing one blood sample. Patients with pneumonia and healthy patients will also be recruited as a control group.

Interventions

OTHERILD

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

OTHERHealthy

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

OTHERPneumonia

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

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Future Disease Management1 visitReliable biomarkers to help guide treatment in ILD would be a major step forward in the management of this disease.

Countries

United States

Contacts

CONTACTMichael Stachowitz
Stachowitz.Michael@mayo.edu507-284-4862
PRINCIPAL_INVESTIGATOREva M Carmona Porquera, MD, PhD

Mayo Clinic

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 30, 2026