New imaging tool could help doctors set ventilators for lung injury patients
NCT ID NCT06823804
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a special imaging method called electrical impedance tomography (EIT) can help doctors choose the best ventilator settings for patients with severe lung injury (ARDS). The goal was to see if EIT could identify which patients would benefit from higher or lower pressure settings, and to spot those at higher risk. The study involved 120 critically ill patients on ventilators. The findings may lead to safer, more personalized breathing support in the ICU.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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120 people
The number who actually took part.
- Started
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Dec 2022
- Finished
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Dec 2024
- 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
This study included adult patients (≥18 years) with moderate-to-severe acute respiratory distress syndrome (ARDS) who were receiving invasive mechanical ventilation in the intensive care unit (ICU) of Ruijin Hospital. All enrolled patients met the Berlin definition of ARDS and had a PaO₂/FiO₂ ratio ≤200 mmHg within 6 hours of screening. A total of 120 patients were consecutively enrolled from December 2022 to December 2024. Patients were stratified by airway closure status for subgroup analyses.
- Ages
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18 to 90 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients who meet the Berlin definition of ARDS and have been treated with mechanical ventilation (clinical diagnosis of ARDS by the attending ICU physician) * PaO₂/FiO₂ ≤200 mmHg Exclusion Criteria: * Age\< 18 or \>90 years * Pneumothorax, pneumomediastinum * Hemodynamic instability (rising vasopressor need in \<6h) * Contraindications to RM or EIT
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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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Department of Critical Care Medicine,Ruijin Hospital,Shanghai Jiao Tong University School of Medicine,Shanghai,China.
Shanghai, Shanghai Municipality, 200025, China
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Other studies related to the condition(s) this trial covers.
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