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

University of Wisconsin (UW) logo

University of Wisconsin (UW)

Status

Completed

Conditions

Sedation

Treatments

Other: SNAP II EEG System

Study type

Observational

Funder types

Other

Identifiers

NCT00204711
SNAPII
H-2005-0014

Details and patient eligibility

About

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.

Enrollment

51 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  • Use of inhalation general anesthesia
  • ASA IV physical status

Trial design

51 participants in 1 patient group

Outpatient Surgery with Sedation
Description:
SNAP II EEG data will be recorded continuously during the sedation and intermittently compared to routinely monitored parameters of sedation adequacy including vital signs, patient movement, grimacing, verbal complaints, and patient responsiveness to verbal and tactile stimuli. Following surgery, patients will be questioned to determine recall or memory of discomfort.
Treatment:
Other: SNAP II EEG System

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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