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Starting soon Observational

Risk of Pneumonia in Intubated Patients in Emergency Situations

NCT07439146 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2026-02-09
Last updated
2026-02-27

Condition(s) studied

PneumoniaOrotracheal Intubation

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adult man or woman * Emergency and non-emergency intubated patient in 2024 * Patient hospitalized in intensive care following intubation in 2024 Exclusion Criteria: * Patient under guardianship, curatorship or safeguard of justice * Pregnant woman * Refusal to participate

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)

FacilityCityRegionStatus
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
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 NCT07439146 on ClinicalTrials.gov ↗ ← All trials in France