Clinical Trial

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

Study acronym: REPEIT
Not Yet Recruiting
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Record status
This record was last updated November 21, 2024 (before its estimated January 2026 completion). Its status may not reflect the trial's current state.
Summary
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.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-08-02.
Trial Details
NCT Number NCT06541522
Lead Sponsor Centre Hospitalier Saint Joseph Saint Luc de Lyon
Conditions ARDS
Enrollment 20 participants
Start Date 2025-01-01
Primary Completion 2026-01 (estimated)
Study Completion 2026-01 (estimated)
Updated on ClinicalTrials.gov 2024-11-21