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New study questions rush to antibiotics for ventilator lung infections
NCT ID NCT06743529
First seen Jun 26, 2026 · Last updated Sep 02, 2026 · Updated 3 times
Summary
This study compares two approaches for treating suspected ventilator-associated pneumonia (VAP) in ICU patients who are not severely ill. One group gets antibiotics immediately, while the other waits for lab confirmation. The goal is to see if waiting reduces unnecessary antibiotic use without increasing deaths or time on a ventilator. About 686 adults on ventilators for more than 48 hours will take part.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- antibiotics
- What this could lead to
- If it works, this could show that waiting for lab confirmation before starting antibiotics is safe for non-severe VAP, reducing unnecessary antibiotic use and fighting resistance.
- What could go wrong
- This is an early-stage trial with 686 participants. The conservative strategy might delay treatment for some infected patients, potentially worsening outcomes. Results may not apply to severe cases.
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 686 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2025
- Expected to finish
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Feb 2029
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: * Invasive mechanical ventilation for longer than 48 hours * Respiratory sample collection taken less than two hours ago (at physician discretion, according to local protocol) for a first episode of suspected ventilator-associated pneumonia (meeting the following prespecified criteria) : * new or changing chest X-ray infiltrates * plus at least two of the following: * body temperature ≥38°C or ≤35.5°C, * blood leukocyte count \>12 000/µL or \<4000/µL, * purulent tracheobronchial aspirate. * Age ≥18 years * Informed consent from the patient or next of kin to participation in the trial, or emergency procedure if no next of kin is available * Patients affiliated to a social security system Non-inclusion Criteria: * Criteria for severe ventilator-associated pneumonia defined as: * Vasopressor therapy for onset of septic shock around the time of ventilator-associated pneumonia suspicion * Onset or severe worsening of hypoxemia (PaO2/FiO2\<150 with 60% FiO2 and 10 mm H2O peak expiratory pressure, or patient on veno-venous extracorporeal membrane oxygenation) * Immunosuppression defined as : * leukocytes \<1G/L or neutrophils \<0,5 G/L * within the last 3 months * hematopoietic stem-cell transplant or organ transplant with chronic immunosuppressant therapy * HIV infection with CD4\<50/mm3 * chronic corticosteroid use (\>0.5 mg/kg day for at least one month within the last three months). * Patient already on Antibiotic Therapy of predicted duration ≥4 weeks (endocarditis, spondylodiscitis, abscess...) * Previous ventilator-associated pneumonia suspicion with sampling and/or Antibiotic Therapy for suspected ventilator-associated pneumonia * Previous inclusion in the trial * Patient included in an interventional study on ventilator-associated pneumonia management with the same primary endpoint. * Pregnancy, recent delivery, or breastfeeding * Correctional facility inmate, adult under guardianship * Patient under legal protection * Life expectancy less than 48 h and/or decision not to treat potential pneumonia acquired under mechanical ventilation in the context of limiting/discontinuing treatment. * Organ donor reanimation
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Get notified about this study
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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
42 sites in 2 countries. 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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APHP - Hôpital Cochin
RECRUITINGParis, 75014, France
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APHP - Hôpital Raymond Poincaré
RECRUITINGGarches, 92380, France
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APHP - Hôpital Tenon
RECRUITINGParis, 75020, France
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CH Angoulème
RECRUITINGAngoulème, France, 16000, France
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CH Argenteuil
RECRUITINGArgenteuil, France, 95100, France
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CH Avignon
RECRUITINGAvignon, 84000, France
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CH Bretagne Atlantique
RECRUITINGVannes, 56017, France
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CH Cholet
RECRUITINGCholet, 49325, France
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CH Dax
RECRUITINGDax, 40107, France
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CH Emile Roux
RECRUITINGLe Puy-en-Velay, 43000, France
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CH Le Mans
RECRUITINGLe Mans, 72000, France
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CH Public du Cotentin
RECRUITINGCherbourg, 50102, France
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CH Simone Veil
RECRUITINGCannes, 06414, France
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CH Versailles
RECRUITINGLe Chesnay, 78157, France
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CH d'Arles
RECRUITINGArles, 13637, France
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CH de Melun
RECRUITINGMelun, 77000, France
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CH de Mont de Marsan
RECRUITINGMont-de-Marsan, 40000, France
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CH de Pau
RECRUITINGPau, 64000, France
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CH de Saint-Malo
RECRUITINGSt-Malo, 35403, France
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CH de Saint-Nazaire
RECRUITINGSaint-Nazaire, 44600, France
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CH de Valenciennes
RECRUITINGValenciennes, 59300, France
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CHD Vendée
RECRUITINGLa Roche-sur-Yon, 85025, France
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CHR d'Orléans
RECRUITINGOrléans, 45100, France
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CHRU De Tours
RECRUITINGTours, 37044, France
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CHRU Lille
RECRUITINGLille, 59037, France
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CHRU de Strasbourg - Nouvel Hôpital Civil
RECRUITINGStrasbourg, 67091, France
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CHRU de Strasbourg -Hôpital de Hautepierre
RECRUITINGStrasbourg, 67098, France
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CHU Angers
RECRUITINGAngers, France, 49000, France
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CHU Clermont-Ferrand
RECRUITINGClermont-Ferrand, 63003, France
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CHU Dijon
RECRUITINGDijon, 21033, France
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CHU La Guadeloupe
RECRUITINGPointe-à-Pitre, 97159, Guadeloupe
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CHU Nantes
RECRUITINGNantes, France, 44000, France
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CHU Nice - Hôpital de l'Archet
RECRUITINGNice, 06200, France
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CHU Nice -Hôpital Pasteur
RECRUITINGNice, 06100, France
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CHU Rennes
RECRUITINGRennes, 35033, France
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CHU de Bordeaux
RECRUITINGBordeaux, 33076, France
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CHU de Bordeaux
RECRUITINGBordeaux, France
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CHU de Lyon - Hôpital Edouard Herriot
RECRUITINGLyon, 69437, France
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GHB Sud- Hôpital de Lorient
RECRUITINGLorient, 56100, France
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Hôpital Européen Marseille
RECRUITINGMarseille, France
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Hôpital Foch
RECRUITINGSuresnes, 92150, France
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Hôpital Nord Franche Comté
RECRUITINGBelfort, 90000, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can tailored antibiotic doses beat resistance in the sickest patients?
- A mist of antibiotic could stop a deadly ICU infection
- Can better nurse training reduce ICU complications?
- Lung germ shifts may predict pneumonia in brain surgery ICU patients
- Can a simple inhaled antibiotic stop ventilator pneumonia?
- Elderly ICU Patients' immune paralysis linked to pneumonia risk