SPIROMICS Study of Early COPD Progression (SOURCE)

NCT05033990 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2025-05-29

No results posted yet for this study

Summary

This is an observational study of 1000 participants to further define the nature of early chronic obstructive pulmonary disease (COPD) in younger, at-risk individuals.

The study has three main goals:

* To use CT scan imaging to identify which smokers will develop COPD.
* To identify biomarkers predictive of smokers that will develop COPD.
* To determine if sputum (phlegm) can be analyzed to predict which smokers will develop COPD.

Procedures (methods): All participants will undergo study related questionnaires assessing medical history, smoke exposure and use, medication use, social and behavioral health, pulmonary symptoms, food frequency, and will provide nasal swab, blood, stool, and urine samples, pulmonary function testing to determine function, sputum induction to provide a sputum sample for airway biospecimen analysis, and CT imaging of the lungs.

Conditions

  • COPD, Early-Onset

Sponsors & Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

    collaborator NIH
  • University of North Carolina, Chapel Hill

    collaborator OTHER
  • Columbia University

    collaborator OTHER
  • Johns Hopkins University

    collaborator OTHER
  • National Jewish Health

    collaborator OTHER
  • University of Alabama at Birmingham

    collaborator OTHER
  • University of California, Los Angeles

    collaborator OTHER
  • University of Illinois at Chicago

    collaborator OTHER
  • University of Iowa

    collaborator OTHER
  • University of Michigan

    collaborator OTHER
  • University of Utah

    collaborator OTHER
  • Wake Forest University Health Sciences

    collaborator OTHER
  • Temple University

    collaborator OTHER
  • University of California, San Francisco

    collaborator OTHER
  • COPD Foundation

    collaborator OTHER
  • Weill Medical College of Cornell University

    collaborator OTHER
  • Mayo Clinic

    collaborator OTHER
  • University of Massachusetts, Worcester

    lead OTHER

Principal Investigators

  • Fernando J Martinez, MD, MS · University of Massachusetts Chan Medical School

  • MeiLan K Han, MD,MS · University of Michigan

  • Jeffrey L Curtis, MD · University of Michigan

Eligibility

Min Age
30 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-09-08
Primary Completion
2026-04-30
Completion
2026-04-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05033990 on ClinicalTrials.gov