Can a warmer, wetter breath during surgery protect the lungs?
NCT ID NCT07729319
First seen Jul 27, 2026 · Last updated Jul 28, 2026 · Updated 1 time
Summary
General anesthesia bypasses the nose's natural warming and moistening of air, letting cold, dry gases reach the lungs. This study compares two humidification methods—active heated humidification versus a passive heat-moisture exchanger—in adults undergoing video-assisted thoracoscopic surgery (VATS) with one-lung ventilation. Researchers will track lung complications within the first week after surgery to see whether either approach is linked to fewer problems.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- active heated humidification or passive heat-moisture exchanger device used during anesthesia
- What this could lead to
- If one method proves better, it could point toward a simple change in anesthesia practice that reduces lung complications after chest surgery.
- What could go wrong
- This is an observational study, not a randomized trial, so results may be influenced by factors other than the humidification method. The devices are chosen by the anesthesiologist, not assigned by the study.
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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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Apr 2027
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.
Who is studied
Adult patients undergoing elective video-assisted thoracoscopic lung resection requiring one-lung ventilation at Marmara University Pendik Training and Research Hospital.
- Ages
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18 to 75 years
- 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: * Patients aged 18 to 75 years * Elective video-assisted thoracoscopic surgery (VATS) * Lung resection requiring general anesthesia * Planned one-lung ventilation * Written informed consent Exclusion Criteria: * Emergency surgery * Pregnancy * Preoperative mechanical ventilation * Previous enrollment * Refusal to participate
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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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Marmara University
RECRUITINGIstanbul, Istanbul, 34722, Turkey (Türkiye)
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