New gas analyzer could spot lung leaks faster
NCT ID NCT06548386
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tests a new, reusable gas analyzer that attaches to chest drains to detect air leaks after lung surgery. The device measures carbon dioxide, oxygen, and pressure to identify leaks, potentially improving accuracy over the current method of watching for bubbles. About 33 adults scheduled for thoracic surgery will participate, and the device will be compared to standard visual inspection.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- pleural gas analyzer (device)
- What this could lead to
- If successful, this device could provide a more accurate and reliable way to detect air leaks after lung surgery, potentially reducing complications and hospital stays.
- What could go wrong
- This is a small, early feasibility study with only 33 participants, so results may not apply to all patients. The device may not be more accurate than current methods.
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 33 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2025
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
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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18 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.
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: 1. Patients who are scheduled for thoracic surgery and expected to have chest tube placed 2. For patients who are unable to sign consent, but meet all of the inclusion criteria and none of the exclusion criteria, a legally appointed representative (LAR) will be allowed to sign consent for that patient 3. Patients that provide informed consent for the study 4. Patients \>18 years old Exclusion Criteria: 1. Patients with hemodynamic instability 2. Pregnant patients 3. Prisoners 4. Individuals who are not yet adults
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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 places running it
1 site. The list below names each one and where it is.
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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.
Contacts and locations
Locations
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Endeavor Health
RECRUITINGEvanston, Illinois, 60201, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- AI eye on X-Rays: could a computer save lives in the ER?