Interstitial Lung Disease Research Unit Biobank

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Kansas Medical Center

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 volunteers

Qualifiers

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

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Collect clinically obtained data for patients with ILD, RLD and risk for ILD/RLD to support research.

Time frame
Enrollment to Year 10
2

Establish a collection of biological samples from patients with ILD, RLD and subjects at risk for ILD.

Time frame
Enrollment to Year 10
3

Correlate biological samples with individual longitudinal clinical data.

Time frame
Enrollment to Year 10
4

Provide biological samples to researchers performing studies in ILD and RLD.

Time frame
Enrollment to Year 10

Secondary outcomes

Other outcomes

Sponsors and contacts

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