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

Recruiting
Conditions
Interstitial Lung Disease
Registration Number
NCT03478826
Lead Sponsor
Mayo Clinic
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.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
635
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

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Future Disease Management1 visit

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

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Mayo Clinic

🇺🇸

Rochester, Minnesota, United States

Mayo Clinic
🇺🇸Rochester, Minnesota, United States
Michael Stachowitz
Contact
507-284-4862
Stachowitz.Michael@mayo.edu
Eva Carmona, M.D., Ph.D.
Contact

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