Endotracheal Suctionning During Positive Pressure Extubation in ICU

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Hospitalier Régional d'Orléans

About this trial

The aim of this clinical trial is to evaluate endotracheal suctioning during positive pressure extubation in mechanically ventilated adult patients (over 18 years old) in the intensive care unit (ICU). The main question it aims to answer is whether the intervention improves the respiratory oxygenation index (ROX) three hours after extubation compared to no endotracheal suction during positive pressure extubation.

Participants will only need to be extubated by the nursing team in the ICU. Follow-up will consist of evaluating respiratory rate, pulse oximetry and inspired oxygen fraction for three hours following extubation.

Eligibility criteria

Qualifiers

Adult patient

Intubated for more than 48 hours

Patient for whom extubation is prescribed by the patient's physician

Disqualifiers

Headboard restriction>30°.

Decision to limit active treatment in advance of reintubation

Protected person (under guardianship or curatorship)

Person under court protection

Trial design

Treatments tested in this trial

  • Suctionning extubation
  • No suctionning Extubation

Treatment groups

120 Participants
are divided into 2 treatment groups