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Clinical Trials in France / NCT06466980
Recruiting Observational

Study of Ventilator Associated Event During Intensive Care After Resuscitated Cardiac Arrest.

NCT06466980 · tracked via the Priya Life Science France tracker
Sponsor
Centre Hospitalier Sud Francilien
Phase
Observational
Started
2024-06-27
Last updated
2025-03-14

Condition(s) studied

Cardiac Arrest With Successful ResuscitationMechanical Ventilation

Investigational drug(s) / intervention(s)

Ventilator associated event

Ventilator associated event: Measure of incidence of Ventilator associated event

Study summary

The aim is to describe the incidence, characteristics, risk factors and outcome of complications acquired under mechanical ventilation (called ventilator-associated events) according to the new CDC criteria, in a population of patients admitted in intensive care unit after cardiac arrest.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adult male or female * Non-pregnant female * Successfully resuscitated from cardiac arrest during primary care * Invasive mechanical ventilation initiated during resuscitation and continued for at least 4 days * No decision to limit life-sustaining therapies within 24 hours following admission to intensive care * No requirement of arteriovenous circulatory support during intensive care management Exclusion Criteria \- patients who opposed to the use of their data

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Centre Hospitalier Sud Francilien Corbeil-Essonnes France Recruiting

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Other trials for the same condition

Impact of an Early and Extended Rehabilitation Program Combining Individually Tailored Nutrition and Physical Activities on Patient Outcomes After Invasive Mechanical Ventilation and Vasopressor Therapy in the ICU Recruiting
Relationship Between the Level of Positive End-expiratory Pressure and Venous Congestion During Acute Respiratory Distress Syndrome. Starting soon
Flow-Controlled Ventilation to Improve Postoperative Pulmonary Outcome After Thoracic Surgery Starting soon
Brain-injured Patients Extubation Readiness Study Recruiting
Simple Mechanical Device to Control Pressure in the Balloon of the Endotracheal Tube to Prevent Ventilator-acquired Pneumonia Recruiting
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 NCT06466980 on ClinicalTrials.gov ↗ ← All trials in France