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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:
Information provided by:
University of Wisconsin, Madison
ClinicalTrials.gov Identifier:
NCT00204711
First received: September 12, 2005
Last updated: December 26, 2007
Last verified: December 2007
  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

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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

No publications provided

Responsible Party: Scott Springman, MD, University of Wisconsin
ClinicalTrials.gov Identifier: NCT00204711     History of Changes
Other Study ID Numbers: 2005-0014, SNAPII
Study First Received: September 12, 2005
Last Updated: December 26, 2007
Health Authority: United States: Institutional Review Board

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

ClinicalTrials.gov processed this record on November 20, 2014