Viewing Study NCT05327296



Ignite Creation Date: 2024-05-06 @ 5:28 PM
Last Modification Date: 2024-10-26 @ 2:30 PM
Study NCT ID: NCT05327296
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2024-06-06
First Post: 2022-04-05

Brief Title: Efficacy and Safety of Inhaled Isoflurane Delivered Via the Sedaconda ACD-S Compared to Intravenous Propofol for Sedation of Mechanically Ventilated Intensive Care Unit Adult Patients INSPiRE-ICU2
Sponsor: Sedana Medical
Organization: Sedana Medical

Study Overview

Official Title: 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 Adult Patients INSPiRE-ICU2
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2024-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: INSPiRE-ICU2
Brief 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
Detailed 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 Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None