Clinical Trials Directory

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

TypeNameDescription
OTHERSNAP II EEG SystemA 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.