Smart oxygen monitoring may reduce lung injury during surgery
NCT ID NCT07359833
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a new monitoring tool called the Oxygen Reserve Index (ORi) to help doctors give just the right amount of oxygen during lung surgery. Sixty adults having lung surgery with one-lung ventilation were randomly assigned to either ORi-guided oxygen management or standard care. The goal was to see if ORi guidance could lower oxygen exposure and reduce markers of oxidative stress and postoperative complications.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Oxygen Reserve Index (ORi)-guided oxygen titration (device)
- What this could lead to
- If successful, this approach could help reduce oxygen-related lung injury during lung surgery, potentially leading to fewer breathing complications after surgery.
- What could go wrong
- This is a small, completed study with only 60 participants. The findings may not apply to all patients or surgeries, and the benefits of ORi guidance remain uncertain without larger trials.
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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60 people
The number who actually took part.
- Started
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Aug 2022
- Finished
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Aug 2023
- 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.
- 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: * Patients age between 18-85 years Elective case Thoracic surgeries performed with one-lung ventilation using a double-lumen endotracheal tube Left ventricule ejection fraction(LVEF)\>45% Exclusion Criteria: * heart failure (LVEF) \< 45% severe valvular disease admission as an emergency case history of prior lung resection presence of peripheral arterial disease.
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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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Gazi University
Ankara, 06560, Turkey (Türkiye)
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