Risk of Pneumonia in Intubated Patients in Emergency Situations
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital, Clermont-Ferrand
About this trial
Orotracheal intubation in emergency medicine is a vital procedure for ensuring adequate oxygenation and ventilation in patients with respiratory distress or in shock. However, this procedure exposes patients to complications such as pneumonia. In the matter of fact, the urgency of the procedure means that it is not possible to wait until the patient's stomach is empty. Pneumonia significantly increase patient morbidity and mortality. Therapeutic management must be early and appropriate to improve the patient's prognosis.
The aim of this study is to compare the rate of pneumonia occurring in patients intubated in emergency situations with that in patients intubated in non-emergency situations in all 2024. Health data will only collected from patient's medical records.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adult man or woman
Emergency and non-emergency intubated patient in 2024
Patient hospitalized in intensive care following intubation in 2024
Disqualifiers
Patient under guardianship, curatorship or safeguard of justice
Pregnant woman
Refusal to participate
Trial population
Study population is patient intubated in emergency situation and patients intubated in non-emergency situation following to the admission of intensive care in 2024.
Trial design
Design model
Cohort
Time perspective
Retrospective
Treatments tested in this trial
Not listed
Trial groups
600 Participants
are grouped into 2 trial groupsGroup A: Intubated patients in emergency situations
Group B: Intubated patients in non emergency situations
Trial outcomes
Primary outcomes
1
Pneumonia rate in 48 hours after the start of orotracheal intubation.
Rate of pneumonia occuring within 48 hours of the start of orotracheal intubation.
Time frame
Hour 48Secondary outcomes
1
Pneumonia rate occuring 48 hours after the start of orotracheal intubation.
Rate of pneumonia occuring more than 48 hours after the start of orotracheal intubation.
Time frame
3 months2
Duration of mechanical ventilation
Duration of mechanical ventilation
Time frame
Up to the end of mechanical ventilation (assessed up to 1 month)3
Duration of stay in intensive care
Duration of stay in intensive care
Time frame
Up to intensive care discharge (assessed up to 1 month)4
Duration of hospital stay
Duration of hospital stay
Time frame
Up to hospital discharge (assessed up to 3 months)Sponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: