Trials / Completed
CompletedNCT00204711
Use of the SNAP II Electroencephalography (EEG) Monitor in Outpatients Undergoing Surgery/Procedures With Sedation
Use of the SNAP II EEG Monitor in Outpatients Undergoing Surgery/Procedures With Sedation
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 51 (actual)
- Sponsor
- University of Wisconsin, Madison · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine if the SNAP II electroencephalography (EEG) monitor accurately reflects changes in sedation level in outpatients undergoing surgery or procedures with sedation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | SNAP II EEG System | A portable EEG monitor (SNAP II EEG System, Everest -St. Louis) is unique in that it monitors both low frequency EEG signals (1-40 Hz), which are typically used, and high frequency EEG signals (80-420 Hz), which are not usually used, and calculates a derived EEG parameter (the SNAP Index). The SNAP Index ranges from 100 (completely awake) to 0 (no brain activity) and has been shown in a few studies to correlate with increasing sedation and loss of consciousness in human volunteers and patients receiving general anesthesia during surgery. |
Timeline
- Start date
- 2005-01-01
- Primary completion
- 2009-11-01
- Completion
- 2009-11-01
- First posted
- 2005-09-20
- Last updated
- 2019-01-24
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00204711. Inclusion in this directory is not an endorsement.