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

  • STATUS
    Recruiting
  • End date
    Jan 20, 2028
  • participants needed
    500
  • sponsor
    Mayo Clinic
Updated on 20 January 2022
pneumonia
pulmonary disease
sarcoidosis
progressive systemic sclerosis
lymphangioleiomyomatosis
Accepts healthy volunteers

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.

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.

Details
Condition Interstitial Lung Disease
Treatment pneumonia, ILD, healthy
Clinical Study IdentifierNCT03478826
SponsorMayo Clinic
Last Modified on20 January 2022

Eligibility

Yes No Not Sure

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
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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