Ultrasound might reveal hidden lung damage in COPD
NCT ID NCT07757126
First seen Aug 11, 2026 · Last updated Aug 12, 2026 · Updated 1 time
Summary
This study is testing whether a simple lung ultrasound can tell the difference between a sudden COPD flare-up and stable disease. It will compare ultrasound images, breathing tests, and exercise ability in about 60 people—those with an acute exacerbation, those with stable COPD, and healthy controls. The goal is to see if ultrasound findings, like B-lines and consolidations, relate to how breathless patients feel and how well they can move. If it works, lung ultrasound could become a quick, non-invasive way to check disease severity at the bedside.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could establish lung ultrasound as a reliable bedside tool to quickly assess COPD severity and guide management.
- What could go wrong
- This is a small, observational study, so results may not apply broadly. Ultrasound findings may not strongly correlate with symptoms or function.
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.
- Participants
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85 people
The number who actually took part.
- Started
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May 2026
- Finished
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Jul 2026
- 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.
Who is studied
Adults aged 40-75 years will be recruited from Munzur University and Tunceli State Hospital. The study population will consist of three groups: patients with acute exacerbation of chronic obstructive pulmonary disease (AECOPD), patients with clinically stable COPD, and age-matched healthy controls. Eligible participants will be enrolled consecutively after providing written informed consent and will undergo standardized assessments, including lung ultrasound, pulmonary function testing, functional capacity tests, dyspnea evaluation, and psychological assessments.
- Ages
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40 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Acute Exacerbation COPD Group * Adults aged 40-65 years. * Diagnosis of chronic obstructive pulmonary disease (COPD) according to GOLD criteria. * Currently experiencing an acute exacerbation of COPD. * Able and willing to provide written informed consent. * Stable COPD Group * Adults aged 40-75 years. * Diagnosis of chronic obstructive pulmonary disease (COPD) according to GOLD criteria. * Clinically stable without an acute exacerbation at the time of assessment. * Able and willing to provide written informed consent. * Healthy Control Group * Adults aged 40-65 years. * No history of chronic pulmonary disease. * Able and willing to provide written informed consent. Exclusion Criteria: * Presence of cardiovascular, neurological, orthopedic, psychiatric, or other systemic diseases that may affect study assessments. * Cognitive impairment or psychological conditions preventing completion of study procedures. * History of thoracic or major surgery that could influence pulmonary function or lung ultrasound findings. * Pregnancy. * Inability to perform pulmonary function testing or functional exercise tests. * Refusal or inability to provide written informed consent.
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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.
Contacts and locations
Locations
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Munzur University Faculty of Health Sciences
Tunceli, Turkey (Türkiye)
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