Leveraging Lung Cancer Screening to Optimize Screening Outcomes and COPD Management: COPD in LCS Registry

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age50-80
SponsorSidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University

About this trial

The COPD in LCS Registry will identify and characterize individuals who have functional or radiographic evidence of COPD and are receiving lung cancer screening. Clinical information will be obtained from study participants including symptom burden, lung cancer risk, spirometry, imaging characteristics, and peripheral blood eosinophils.

Eligibility criteria

Qualifiers

• * 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

Disqualifiers

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). We 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

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed