Study of Ventilator Associated Event During Intensive Care After Resuscitated Cardiac Arrest.
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Hospitalier Sud Francilien
About this trial
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 criteria
This trial does not accept healthy volunteersQualifiers
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
Disqualifiers
None
Trial population
Patient admitted to intensive care unit after cardiac arrest at the South Francilien Hospital Center from January 2019 to December 2023
Trial design
Design model
Cohort
Time perspective
Other
Treatments tested in this trial
Ventilator associated event
Other interventionMeasure of incidence of Ventilator associated event
Treatment groups
No treatment groups listed
Trial outcomes
Primary outcomes
1
number
Incidence of ventilator associated event
Time frame
at day 28Secondary outcomes
1
Associated factors
Associated factors of ventilator associated event
Time frame
at day 282
number of pneumonias
Ventilator associated pneumonia according to the American Thoracic Society definition
Time frame
at day 283
time
Mechanical ventilation duration
Time frame
at day 284
number of deaths
In-hospital mortality
Time frame
at day 28Sponsors and contacts
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Source ClinicalTrials.gov