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CompletedNCT01768416

Measuring Depth of Unconsciousness at the End of Life Using Bispectral Index (BIS)

Measuring Depth of Unconsciousness at the End of Life: the Reliability of the BIS Monitoring as an Assessment Tool Versus Sedation Scales

Status
Completed
Phase
Study type
Observational
Enrollment
10 (actual)
Sponsor
University Hospital, Ghent · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to use the BIS monitor to assess the degree of consciousness in pre-terminal palliative patients admitted to our palliative care unit and to ascertain if this tool provides a more accurate assessment of consciousness in this specific group of patients than clinical observation of consciousness and the use of sedation scales. We hypothesize that the measured BIS results provide a more accurate assessment of the patient's level of consciousness than routine clinical observation or the use of sedation scales.

Conditions

Timeline

Start date
2013-03-01
Primary completion
2015-09-23
Completion
2015-09-23
First posted
2013-01-15
Last updated
2023-01-04

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT01768416. Inclusion in this directory is not an endorsement.

Measuring Depth of Unconsciousness at the End of Life Using Bispectral Index (BIS) (NCT01768416) · Clinical Trials Directory