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Use of the SNAP II Electroencephalography (EEG) Monitor in Outpatients Undergoing Surgery/Procedures With Sedation

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00204711
First Posted: September 20, 2005
Last Update Posted: January 4, 2008
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
University of Wisconsin, Madison
  Purpose
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.

Condition
Sedation

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Use of the SNAP II EEG Monitor in Outpatients Undergoing Surgery/Procedures With Sedation

Further study details as provided by University of Wisconsin, Madison:

Estimated Enrollment: 50
Study Start Date: January 2005
Study Completion Date: November 2006
Estimated Primary Completion Date: June 2008 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • American Society of Anesthesiologists (ASA) I, II or III physical status

Exclusion Criteria:

  • Use of inhalation general anesthesia
  • ASA IV physical status
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00204711


Locations
United States, Wisconsin
University of Wisconsin Hospital and Clinics
Madison, Wisconsin, United States, 53792
Sponsors and Collaborators
University of Wisconsin, Madison
Investigators
Principal Investigator: Scott Springman, MD University of Wisconsin, Madison
  More Information

Responsible Party: Scott Springman, MD, University of Wisconsin
ClinicalTrials.gov Identifier: NCT00204711     History of Changes
Other Study ID Numbers: 2005-0014
SNAPII
First Submitted: September 12, 2005
First Posted: September 20, 2005
Last Update Posted: January 4, 2008
Last Verified: December 2007

Keywords provided by University of Wisconsin, Madison:
patients having outpatient surgery with sedation
patients having procedures with sedation