Risk of Pneumonia in Intubated Patients in Emergency Situations
Condition(s) studied
Study summary
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
Primary outcome measure(s)
- Pneumonia rate in 48 hours after the start of orotracheal intubation. — Hour 48
Rate of pneumonia occuring within 48 hours of the start of orotracheal intubation.
Trial sites (6)
| Facility | City | Region | Status |
|---|---|---|---|
| CH Aurillac | Aurillac | France | |
| CHU de Clermont-Ferrand, Clermont-Ferrand | Clermont-Ferrand | France | |
| CH du Puy en Velay | Le Puy-en-Velay | France | |
| CH de Montluçon | Montluçon | France | |
| CH de Moulins | Moulins | France | |
| CH de Vichy | Vichy | France |
More University Hospital, Clermont-Ferrand trials in France
Other trials for the same condition
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 NCT07439146 on ClinicalTrials.gov ↗ ← All trials in France