Scientists investigate why ventilators may worsen lung infections
NCT ID NCT03955887
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at how mechanical ventilation (breathing machines) affects the energy centers (mitochondria) of immune cells in patients with severe lung infections and acute respiratory distress syndrome (ARDS). Researchers aimed to understand why some patients get worse despite treatment. The study was terminated early and involved 28 adults. No direct treatment was given; it was purely observational to gather knowledge for future therapies.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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28 people
The number who actually took part.
- Started
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Jun 2019
- Finished
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May 2020
- 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
Patients admited in the Intensive Care Unit and the Pneumology Intensive Care Unit of the CHU Dijon Bourgogne
- 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: * Patient who has given his non-opposition (or non-opposition obtained from close relative of ventilated patients, who will be informed as soon as possible). * Adult patient * Group 1: patient with: * Acute pneumonitis defined by: Signs and acute symptoms of pneumonia (new or worsening within the last 7 days), at least 2 of which are: * Coughing * Purulent sputum * Dyspnea * Chest pain * Temperature \< 35°C or ≥ 38°C And a new pulmonary radiological infiltrate (x-ray or CT scan on admission) * Not acquired under mechanical ventilation * Complicated from ARDS according to the new Berlin definition, Chest x-ray finding bilateral parenchymal opacities not fully explained by pleural effusions, nodules or atelectasis. Respiratory distress not explained by cardiac dysfunction or overfilling. An echocardiogram will be performed in case of diagnostic uncertainty. PaO2/FiO2 report \< 300 and PEP ≥ 5 cmH2O * Requiring the use of MV. * With a diagnostic BAL performed within 72 hours of the start of the MV * Group 2: Patients: * No fever during the last 15 days (reported or measured ≥ 37.8°C). * Not under MV, * Undergoing BAL for a reason other than acute infection (e.g. chronic interstitial syndrome, nodule or lung mass). Exclusion Criteria: * Patient not affiliated to the national health insurance system * Major under judicial protection * Pregnant, parturient or breastfeeding woman * Known primary or secondary immune deficiency (radiotherapy, chemotherapy, immunosuppressive therapy or systemic corticosteroid therapy (\>10mg/day prednisone equivalent for more than 7 days) within 6 months before inclusion, HIV infection, primary cellular immune deficiency) * Patients with treatment known to modulate mitochondrial function, biogenesis and/or mitophagia (chloroquine, hydroxychloroquine, rapamycin, carbamazepine, resveratrol, metformin, sildenafil) * Patients with pulmonary fibrosis or cystic fibrosis known to be associated with mitochondrial alterations
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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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Chu Dijon Bourogne
Dijon, 21000, France
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Other studies related to the condition(s) this trial covers.
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