Lung imaging could supercharge Post-Surgery breathing exercises

NCT ID NCT07681232

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Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
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Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

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Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
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Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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Status unknown
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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

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

About 60 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

Dec 2027

An estimate. End dates often move.

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

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

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

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How to take part

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Contacts and locations

Locations

  • Zhongshan Hospital, Fudan University

    Shanghai, Shanghai Municipality, 200032, China

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