Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Enhanced COPD care for people being checked for lung cancer

Official title: Enhanced COPD Management in Suspected Lung Cancer Patients - Improving Outcomes Through Timely Intervention

Run by Region of Southern Denmark · NCT07543601 · Data updated 2026-11-12

This project will test whether finding and treating COPD early in people being checked for possible lung cancer helps symptoms, lung function, and overall care.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment280 (estimated)
SponsorRegion of Southern Denmark
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Vejle)
StatusRecruiting
StartedMarch 6, 2026
Main results expectedJune 30, 2027
Study endsJune 30, 2027
Registry record updatedApril 22, 2026
Trial IDNCT07543601 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults undergoing diagnostic evaluation for suspected lung cancer who have spirometry-confirmed obstructive airflow limitation at the first outpatient visit.

Probably not a fit

Patients without obstructive spirometry, those with significant comorbidities that interfere with spirometry or diagnostic procedures, pregnant or breastfeeding women, and patients already receiving optimal COPD care are less likely to benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This open-label randomized controlled trial at the Lung Cancer Investigation Unit, Lillebaelt Hospital Vejle, compares tailored COPD consultations and early optimal COPD treatment to usual care in patients undergoing diagnostic evaluation for suspected lung cancer. Eligible participants must have spirometry-confirmed obstructive airflow limitation at the first outpatient visit and will receive personalized inhaler optimization, smoking-cessation support, and structured follow-up based on COPD severity. The trial will measure changes in health status and lung function as primary outcomes, with secondary outcomes including healthcare utilization, completion of the diagnostic pathway, and survival-related metrics. Clinical, functional, and health-economic data will be combined to determine whether integrated COPD management improves outcomes during the lung cancer diagnostic process.

Why it matters

Potential benefit: If successful, this approach could improve symptoms and lung function, reduce hospital visits and costs, and possibly improve survival for patients evaluated for lung cancer.

How similar studies have gone: Integrated COPD management has improved outcomes in general COPD populations, but randomized evidence specifically targeting patients during lung cancer diagnostic work-ups is limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Undergoing diagnostic evaluation for suspected lung cancer
* Spirometry showing obstructive airflow limitation (FEV₁/FVC \< 75 % or FEV₁ \< 80 %, and no reversibility) at the first outpatient visit at the lung cancer evaluation

Exclusion Criteria:

* Presence of significant comorbidities that may interfere with diagnostic procedures or spirometry
* Pregnant or breastfeeding women

Where it's running

  • Lung Cancer Investigation Unit, Lillebaelt Hospital Vejle
    Vejle, Denmark
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.