drugset / Trial / NCT04235608
SEvoflurane for Sedation in ARds
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Propofol | Small molecule | — | Intravenous |
| Subject | Sevoflurane | Other / unclassified | — | Inhaled |