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Clinical Trial Summary

This is a study to compare safety and efficacy of inhaled isoflurane administered via the Sedaconda ACD-S device system versus intravenous propofol for sedation of mechanically ventilated patients in the Intensive Care Unit (ICU) setting.


Clinical Trial Description

This is a phase 3, multicenter, randomized, controlled, open-label, assessor-blinded study to evaluate the efficacy and safety of inhaled isoflurane delivered via the Sedaconda ACD-S compared to intravenous propofol for sedation of mechanically ventilated Intensive Care Unit (ICU) adult patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05312385
Study type Interventional
Source Sedana Medical
Contact
Status Active, not recruiting
Phase Phase 3
Start date April 28, 2022
Completion date October 30, 2024

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