Impact of Belt Position on the Results of PEEP Titration by EIT During ARDS

ConditionARDS
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Hospitalier Saint Joseph Saint Luc de Lyon

About this trial

ARDS is a frequent reason for hospitalization in intensive care. In order to improve its management, doctors seek to limit the mechanical ventilation-induced injuries (VILI) that can occur. PEEP is a parameter that plays a role in the appearance of VILI, and its adjustment can be optimized by EIT. The EIT is a non-invasive, non-irradiating, real-time monitoring device, today widely used for the optimization of ventilation in patients intubated for ARDS. The positioning of the EIT belt at different chest heights could influence the result of the PEEP titration.

Eligibility criteria

Qualifiers

Occurrence of moderate to severe ARDS (PaO2/FiO2 ratio ≤ 200 mmHg) within 72 hours following intubation

Criteria for moderate to severe ARDS for less than 72 hours

Passive ventilation in controlled assisted ventilation (no spontaneous ventilation)

Consent of next of kin

Disqualifiers

Age < 18 years

ECMO

Pneumothorax

Pacemaker or implantable defibrillator

Trial design

Treatments tested in this trial

  • EIT

Treatment groups

20 Participants
are divided into 1 treatment group

Locations

This trial has no locations