Lung imaging could supercharge Post-Surgery breathing exercises
NCT ID NCT07681232
First seen Jul 02, 2026 · Last updated Jul 02, 2026
Summary
This trial investigates whether showing patients real-time images of their lungs during breathing exercises helps air reach collapsed areas more effectively. Adults who have had major chest or upper-abdominal surgery and have lung collapse (atelectasis) will perform breathing exercises with or without visual feedback from a device called electrical impedance tomography. The study aims to see if this feedback improves ventilation distribution in the lungs.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- EIT-guided visual feedback during incentive spirometry
- What this could lead to
- If effective, this approach could help patients recover lung function more quickly after surgery by improving how air reaches collapsed areas.
- What could go wrong
- This is a small, early-stage trial with only 60 participants, so results may not apply to all patients. The technique requires specialized equipment and training.
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 60 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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Dec 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.
- 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. Age 18 years or older. 2. Admitted to an intensive care unit or postoperative monitoring unit after major thoracic or upper-abdominal surgery; tracheal tube removed; spontaneously breathing; and clinically stable. 3. Alert and able to understand and follow incentive-spirometry and EIT instructions. 4. Bedside lung ultrasound shows atelectasis or markedly reduced aeration in dorsal or posterolateral lung regions, with the lung-ultrasound assessment recorded. 5. Baseline EIT during quiet breathing in a semi-recumbent position shows insufficient dorsal ventilation with potential for improvement; dorsal ventilation fraction below 50%. 6. Written informed consent provided by the participant or legally authorized representative according to the ethics-approved process, with participant re-consent when decision-making capacity returns. Exclusion Criteria: 1. Ongoing invasive mechanical ventilation or noninvasive ventilation, or high-flow nasal oxygen when study conditions cannot be maintained stably. 2. Hemodynamic instability or inability to tolerate a semi-recumbent position. 3. Inability to cooperate with training or impaired consciousness. 4. Unsuitable for EIT monitoring, including an implanted pacemaker or defibrillator incompatible with the device, severe skin disease at the electrode-belt site, or known relevant allergy. 5. Severe underlying pulmonary disease likely to substantially affect ventilation distribution and obscure the intervention effect. 6. Chest-wall deformity or severe scoliosis affecting EIT image quality. 7. Body mass index greater than 35 kg/m2. 8. Pregnancy or breastfeeding. 9. Current participation in another interventional clinical trial that could interfere with study outcomes. 10. Any other condition that, in the investigator's judgment, makes participation inappropriate.
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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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Zhongshan Hospital, Fudan University
Shanghai, Shanghai Municipality, 200032, China
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Other studies related to the condition(s) this trial covers.
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- High-Flow oxygen may shield lungs after keyhole surgery
- Ultrasound reveals best position to avoid lung collapse during surgery
- Study aims to solve debate over best ventilator setting to keep lungs open after surgery
- New study tests best way to keep lungs open during surgery