Gentle lung breathing during bypass may prevent Post-Surgery collapse
NCT ID NCT02070445
First seen Jul 10, 2026 · Last updated Jul 10, 2026
Summary
This pilot study tests whether keeping the lungs gently ventilated during cardiopulmonary bypass (heart-lung machine) reduces lung collapse after heart surgery. Adults having elective coronary artery bypass surgery will be randomly assigned to receive ventilation or not during bypass. Lung ultrasound scans will measure collapse at several time points before and after surgery. The study also looks at infection rates, time on the breathing tube, hospital stay length, and blood oxygen levels.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- mechanical ventilation during cardiopulmonary bypass
- What this could lead to
- If keeping the lungs ventilated during bypass reduces lung collapse, it could lead to faster recovery and fewer lung complications after heart surgery.
- What could go wrong
- This is a small pilot study focused on feasibility, not proof of benefit. The approach may not show a meaningful difference or may not be practical in busy surgical settings.
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.
- Expected to start
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Jun 2019
An estimate. Start dates often move.
- Expected to finish
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Dec 2020
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
Same Day Surgery Clinic
- Ages
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18 to 85 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: * Adult elective coronary artery bypass surgery requiring CPB Exclusion Criteria: * Cardiac surgery without CPB * Complex cardiac surgery (valve repairs, combined bypass and valve repairs etc.) * Emergency cardiac surgery * Fibrotic lung disease * Previous lung volume reduction surgery (CXR will be assessed pre-operatively) * Massive blood product transfusion intra- and/or post-operatively will exclude patient * Patients enrolled in other studies eg. SIRS study (steroid use)
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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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Hamilton General Hospital
Hamilton, Ontario, L8L 2X2, Canada
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- SMART-I: SiroMax™ Multi-Center coronary artery lesion treatment - safety and feasibility study of SiroMax SCB in ISR and DNSV
- Hospital-to-Home transitional cardiac rehabilitation as a transition from Centre-Based cardiac rehabilitation after cardiac surgery: a Single-Blind randomised controlled trial
- Opportunistic screening of coronary artery calcium on Non-Gated routine chest CT using artificial intelligence: retrospective external validation and clinical risk stratification
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- Can personalized breathing settings protect lungs during heart surgery?