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NCT07482475Recruiting

University of Michigan COPD Identification Through Lung Cancer Screening Cohort Study - MAP2

Source: ClinicalTrials.gov · Last updated 25 Mar 2026

Brief summary (registry, in English)

The purpose of this study is to obtain new knowledge regarding screening for COPD. This study will use a participant's cancer screening CT scans performed as part of routine health care among current and former smokers at risk for COPD to identify participants who have had a spirometry or will have a spirometry test as part of the study to verify COPD status.

Status (registry)
Recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
1 Feb 2026
Start date
15 Jul 2025
Primary completion date
Dec 2026
Lead sponsor
University of Michigan
Diseases
COPD, Lung cancer
NCT number
NCT07482475

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 15 Jul 2025 to the primary completion date, Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Severe asthma, which is defined as any of the following:
    • Current (i.e. at the time of the visit) GINA Step 4 or higher therapy (medium dose ICS/LABA or high dose ICS or add-on LAMA; Medium dose = \>250 fluticasone propionate =100 fluticasone furoate, \>200 beclomethasone, \>400 budesonide, \>220 mometasone). The investigators will accept low-dose ICS/LABA or medium dose ICS.
    • or 3 or more unscheduled healthcare visits (provider/urgent care/ER) for asthma in the past 12 months or One asthma hospitalization in the past 12 months
  • Concurrent participation in a therapeutic trial where treatment is blinded.
  • Participants who present with an acute exacerbation of COPD, either solely participant-identified or that has been clinically treated, in the last 30 days can be rescreened for the study once the 30-day window from end of drug therapy has passed.
  • Participants who present with current use of acute antibiotics or steroids can be rescreened for the study ≥30 days after discontinuing acute antibiotics/steroids. This restriction does not apply to participants who are on chronic prednisone therapy of \<10 mg per day or \<20 mg every other day or participants who are currently on chronic, prophylactic, or suppressive antibiotic therapy.

Other illness

  • The presence of a respiratory condition other than COPD or asthma, or of a comorbid condition that in the judgment of the investigator may be the principal cause of respiratory symptoms (e.g. dyspnea or decreased exercise tolerance).
  • Any illness expected to cause mortality in the next 3 years.
  • History of thoracic radiation or thoracic surgery with resection of lung tissue.
    • Additional temporal exclusion criteria are as follows:

Other

  • Active pregnancy. Documentation of birth control will be required for pre-menopausal women.
  • Cognitive dysfunction that prevents the participant from completing study procedures.
  • BMI \> 35 kg/m2 at baseline, due to the effects of body weight on CT scan quality.
  • Current illicit substance abuse, including cannabis smoking.
  • Any implanted metallic devices or prosthesis above the waist that could degrade thoracic CT scan quality.

Who the study is looking for

  • Eligible for lung cancer screening by USPSTF 2021 criteria including age 50-80 years and currently or formerly smoking with at last 20 pack-years of smoking history at the time of consent.
  • Willingness to participate in an observational clinical trial and to be contacted about future ancillary studies that could include interventional clinical trials.
  • Ability to tolerate study procedures.
  • Ability to provide informed consent.
  • Clinical Lung Cancer Screening CT performed at the University of Michigan within the last year
  • Meets one of the three following criteria:
    • Prior Diagnosis of COPD in the EMR
    • Prior pulmonary function meeting criteria for COPD (FEV1/FVC ≤ 0.70) or
    • LAA\>1% on lung cancer screening CT scan

Age in the registry: 50 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
University of Michigan
Coordinator of this site? Confirm its status
Ann ArborUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.