New study aims to improve COPD care by checking the heart too
NCT ID NCT07481825
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether adding a thorough heart evaluation to standard lung care helps people with mild-to-moderate COPD who also have heart risks. About 350 adults will be randomly assigned to either the combined heart-lung check or usual respiratory care. The goal is to see if the combined approach improves heart function, exercise ability, and quality of life over 12 months.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- structured combined cardio-pulmonary clinical management strategy
- What this could lead to
- If it works, this could lead to a better way to manage COPD patients who also have heart problems, potentially improving their heart function and daily life.
- What could go wrong
- This is an early-stage study with no results yet. The added heart tests may not lead to better outcomes, and the findings may not apply to all COPD patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 350 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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41 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Patients enrolled in the study should be diagnosed as COPD according to international recommendations (1) with the following features: * Post-bronchodilator FEV1 ≥ 50% or FEV1 z ≥ -2.5 * Age \> 40 years Additionally, enrolled patients must fulfill at least one of the following cardiovascular criteria: * Very high cardiovascular risk * according to SCORE2 (12)for patient \< 70 years old and defined as follows: * Patients \< 50 years old \> 7.5% * Patients 50-69 years old \> 10% * according to SCORE OP 2 (13) calculator for patients \> 70 years old and defined as \> 15% * History of ischemic heart disease * Chronic or transient atrial fibrillation * Chronic heart failure with preserved (HFpEF) or mildly reduced (HFmrEF) ejection fraction (EF \> 40%) (14) Exclusion Criteria: * Post-bronchodilator FEV1 \< 50% or FEV1 z \< -2.5 * LTOLT * Active neoplasm * Patient unable to perform lung function * Pregnancy
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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