Creating a blood sample repository for patients with interstitial lung diseases

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to establish a biospecimen repository by collecting blood samples from patients diagnosed with interstitial lung diseases (ILD), as well as from patients with pneumonia and healthy individuals for comparison. The goal is to gather a total of 500 samples from ILD patients to facilitate future research into potential biomarkers associated with these conditions. By analyzing these samples, researchers hope to gain insights that could lead to improved understanding and treatment of ILD.

Why it matters

Who can join: the full rules

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

Where it's running

• Mayo Clinic
  Rochester, Minnesota, United States Recruiting

Study contacts

• Principal investigator: Eva M Carmona Porquera, MD, PhD — Mayo Clinic
• Study coordinator: Michael Stachowitz
• Email: Stachowitz.Michael@mayo.edu
• Phone: 507-284-4862

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.