Clinical trial
The SOMNUS Study: Sedative Optimization Via Monitoring Neurological Status
NCT00469482 · Vanderbilt University Medical Center, Other · Completed
Key facts
| NCT number | NCT00469482 |
|---|---|
| Title | The SOMNUS Study: Sedative Optimization Via Monitoring Neurological Status |
| Official title | A Randomized Control Trial Using the BIS Monitor to Avoid Over Sedation and Prolonged Neuropsychological Deficits in Mechanically Ventilated ICU Patients |
| Acronym | SOMNUS |
| Lead sponsor | Vanderbilt University Medical Center, Other |
| Collaborators | Medtronic - MITG Industry |
| Status | Completed |
| Study type | Interventional |
| Conditions | Delirium, Cognitive Impairment, Critically Ill |
| Intervention type | Other |
| Interventions | Sedation, RASS Targeted plus BIS Monitoring, RASS Targeted |
| Enrollment | 28 |
| Start date | Jun 1, 2007 |
| Primary completion | Oct 1, 2008 |
| Completion | Sep 1, 2016 |
| First posted | May 4, 2007 |
| Last update posted | Mar 8, 2018 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: