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Ultrasound might reveal hidden lung damage in COPD

NCT ID NCT07757126

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

85 people

The number who actually took part.

Started

May 2026

Finished

Jul 2026

Lead sponsor

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

40 to 75 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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

  • Munzur University Faculty of Health Sciences

    Tunceli, Turkey (Türkiye)

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