drugset / Trial / NCT02166853

Effects of SEvoflurane on Gas Exchange and Inflammation in Patients With ARDS (SEGA Study)

NCT02166853 ↗

Phase 4 Completed 50 enrolled University Hospital, Clermont-Ferrand
RandomizedParallel-groupOpen-labelTreatment

Summary

Numerous trials support the efficacy and safety of volatile anesthetic agents, namely inhalation of sevoflurane through dedicated devices, for the sedation of ICU patients. Several preclinical studies have shown that sevoflurane inhalation improves gas exchange and decreases pulmonary and systemic inflammation in experimental models of acute respiratory distress syndrome (ARDS). The purpose of our prospective monocentric, randomized, controlled trial is to evaluate the effects of an early 48-hour sevoflurane inhalation on gas exchange and inflammation in patients with ARDS.

Timeline

Start
2014-04
Primary completion
2016-02
Completion
2016-03

Outcome

Met primary endpoint

paper On Day 2, PaO2/FiO2 ratio was higher in the sevoflurane group than in the midazolam group (mean ± SD, 205 ± 56 vs. 166 ± 59, respectively; P = 0.04). PMID 27611637 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Midazolam Small molecule — Intravenous
Subject Sevoflurane Other / unclassified — Inhaled