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Clinical Trials in France / NCT05578742
Recruiting Not applicable

V/Q Matching Variations With PEEP in ARDS According to Compliance-based Phenotypes (France)

NCT05578742 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2024-02-08
Last updated
2025-12-08

Condition(s) studied

ARDS

Investigational drug(s) / intervention(s)

PEEP increasePEEP decrease

PEEP increase: Positive End Expiratory Pressure (PEEP) will be increased from 5 to 15 cmH2O.

PEEP decrease: Positive End Expiratory Pressure (PEEP) will be decreased from 15 to 5 cmH2O.

Study summary

This study aim to compare the effect of Positive End Expiratory Pressure (PEEP) on ventilation/perfusion mismatch in two phenotypes of patients with moderate-to-severe Acute Respiratory Distress Syndrome (ARDS), characterized by their respiratory system elastance (Ers). Ventilation/perfusion mismatch will be assessed by Electrical Impedance Tomography (EIT).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion criteria: * intubated patients with moderate and severe ARDS (Berlin definition, PaO2/FiO2 ≤200 mmHg at PEEP 5 cmH2O) * undergoing deep sedation * on controlled mechanical ventilation * between 24 hours and 5 days after intubation. Exclusion criteria: * age \<18 years old; pregnancy * patient undergoing legal protection * contra-indications to EIT (e. g. severe chest trauma or wounds) * pneumothorax; patient undergoing ECMO * patient with BMI ≥35 kg/m2 * hemodynamic instability with MAP \<60 mmHg despite vasopressors.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Angers Hospital Angers Maine et Loire Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05578742 on ClinicalTrials.gov ↗ ← All trials in France