About this trial
Establish a interstitial lung disease (ILD) registry and biorepository to lead towards a further understanding of the disease.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
The participant is a patient at TUKHS or has agreed to participate in a study approved by the KUMC Human Research Protection Program (HRPP)
The participant is being followed for the presence of autoimmune disease, ILD or other rare lung diseases at TUKHS.
The participant is ≥ 18 years of age.
The participant has signed an approved consent for this study (living patients only)
Disqualifiers
None
Trial population
Patients with ILD, RLD and subjects at risk for ILD
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Collect clinically obtained data for patients with ILD, RLD and risk for ILD/RLD to support research.
Establish a collection of biological samples from patients with ILD, RLD and subjects at risk for ILD.
Correlate biological samples with individual longitudinal clinical data.
Provide biological samples to researchers performing studies in ILD and RLD.
Sponsors and contacts
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