Trials / Unknown
UnknownNCT04014218
Effect of Inhalation Sedation Compared With Propofol on the Sepsis-related Acute Respiratory Distress Syndrome Course
Effect of Inhalation Sedation With Sevoflurane Compared With Propofol on the Sepsis-related Acute Respiratory Distress Syndrome (ARDS) Course.
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 80 (estimated)
- Sponsor
- Moscow Regional Research and Clinical Institute (MONIKI) · Other Government
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
Investigation of effect of inhalation sedation by administration of Sevoflurane compared with Propofol on the moderate acute respiratory distress syndrome course in mechanically ventilated patients with sepsis.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Inhalation Sedation | Inhalation Sedation by Administration of Sevoflurane |
| DRUG | Intravenous Sedation | Intravenous Sedation by Administration of Propofol |
Timeline
- Start date
- 2019-01-08
- Primary completion
- 2019-09-01
- Completion
- 2020-01-01
- First posted
- 2019-07-10
- Last updated
- 2019-07-10
Locations
1 site across 1 country: Russia
Source: ClinicalTrials.gov record NCT04014218. Inclusion in this directory is not an endorsement.