drugset / Trial / NCT04235608

SEvoflurane for Sedation in ARds

NCT04235608

Phase 3 Completed 700 enrolled University Hospital, Clermont-Ferrand
RandomizedParallel-groupSingle-blindTreatment

Summary

This study evaluates whether a sedation with inhaled sevoflurane will decrease mortality and increase time off the ventilator at 28 days in patients with acute respiratory distress syndrome (ARDS). Half of the patients will receive inhaled sedation with sevoflurane and the other half will receive intravenous sedation with propofol.

Timeline

Start
2020-05-03
Primary completion
2023-10-31
Completion
2024-10-02

Drugs

EvaluationDrugModalityDoseRoute
Comparator Propofol Small molecule Intravenous
Subject Sevoflurane Other / unclassified Inhaled