New lung therapy may help ventilated patients recover faster
NCT ID NCT07453966
First seen Jun 27, 2026 · Last updated Aug 13, 2026 · Updated 2 times
Summary
This study tests whether adding a special breathing treatment called intrapulmonary percussive ventilation (IPV) to standard care helps patients with pneumonia who are on a breathing machine. About 96 adults will be randomly assigned to receive either standard therapy alone or standard therapy plus IPV. Researchers will monitor lung function, oxygen levels, and how quickly patients can be taken off the ventilator, aiming to see if IPV speeds recovery and is safe.
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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 110 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2026
- Expected to finish
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May 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.
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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: 1. Age ≥ 18 years; 2. Meeting the diagnostic criteria for pulmonary infection, defined as follows: meeting the diagnostic criteria for hospital-acquired pneumonia (HAP) or ventilator-associated pneumonia (VAP) according to the Chinese Guidelines for the Diagnosis and Treatment of Hospital-Acquired Pneumonia and Ventilator-Associated Pneumonia in Adults (2018 edition), or meeting the diagnostic criteria for community-acquired pneumonia (CAP) according to the Chinese Guidelines for the Diagnosis and Treatment of Community-Acquired Pneumonia in Adults (2016 edition); 3. Oxygenation index (PaO₂/FiO₂) ≤ 300; 4. Currently receiving invasive mechanical ventilation, with no planned liberation from invasive mechanical ventilation within the next 24 hours; 5. Receiving analgesia and sedation; 6. Written informed consent provided by the patient's family member or legally authorized representative. Exclusion Criteria: 1. Presence of severe hemodynamic instability (norepinephrine dose \> 0.5 μg/kg/min); 2. Markedly elevated intracranial pressure (\> 25 mmHg) or a condition requiring strict intracranial pressure control; 3. Severe pulmonary bullae, untreated tension pneumothorax or undrained mediastinal emphysema; 4. Unstable chest wall, flail chest, recent thoracic or airway surgery, or severe thoracic spine injury; 5. Active massive hemoptysis; 6. Severe bronchospasm or inability to tolerate fluctuations in airway pressure; 7. Inability to place the EIT chest belt, such as open thoracic surgical wounds or skin lesions at the belt placement site; 8. Receiving extracorporeal membrane oxygenation (ECMO); 9. Acute exacerbation of chronic obstructive pulmonary disease as the primary reason for the current episode of invasive mechanical ventilation; 10. Expected death within 24 hours, or a decision already made to withhold or withdraw life-sustaining treatment; 11. Pregnancy or breastfeeding; 12. Concurrent participation in another clinical trial.
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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.
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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Zhongnan Hospital of Wuhan University
RECRUITINGWuhan, Hubei, 430071, China
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Other studies related to the condition(s) this trial covers.
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