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Deployment-Related Lung Disease Research Database and Biorepository

Deployment-Related Lung Disease Research Database and Biorepository

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03035097
Enrollment
500
Registered
2017-01-27
Start date
2013-02-01
Completion date
2030-12-01
Last updated
2026-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bronchiolitis

Brief summary

The purpose of this research study is to establish a research database and biorepository for patients at National Jewish Health (NJH) who served in Operation Iraqi Freedom (OIF) or Operation Enduring Freedom (OEF). This study will also include civilian contractors who worked as part of these military operations in Iraq or Afghanistan. The biorepository would store blood samples obtained from these patients during a clinic visit. The research database would store prospectively and retrospectively collected clinical and exposure data that would enable us to comprehensively characterize each case.

Detailed description

If informed consent is obtained, test results and other information collected for clinical reasons will be entered in a research database designed and maintained by DEOHS staff. The clinical data collected are part of the routine diagnosis and care of these patients. No additional procedures are required for the purpose of this research database. Collection of symptom and exposure data using a questionnaire designed for this study. All NJH patients who served in southwest Asia will be approached for inclusion in the study. This will also attempt to contact patients evaluated previously at NJH for deployment-related lung disease to obtain informed consent to include data from their medical record and the research questionnaire in the database.

Interventions

One-time blood draw for blood to be stored in a biorepositoy

Sponsors

National Jewish Health
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Served in the southwest Asia wars

Exclusion criteria

* Did not served in the southwest Asia wars

Design outcomes

Primary

MeasureTime frameDescription
collect symptom and exposure dataUp to 24 monthseach subject will complete a questionnaire

Countries

United States

Contacts

CONTACTLauren Zell-Baran, PhD, MPH
zell-baranl@njhealth.org303-398-1187

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 16, 2026