At a glance
ClinicalIndex Comparison RecordN/ACompleted· 300 enrolled
Drug / intervention
Bispectral Index (BIS) Monitordevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Combining Objective and Subjective Sedation Assessment Tools - Second Study
In Brief
A clinical study evaluating Bispectral Index (BIS) Monitor for Critical Illness. Completed, enrolled 300 participants across 1 site.
Detailed Summary
The purpose of this study is to determine if the use of a device called the BIS monitor in addition to the Richmond Agitation Sedation Scale will give better assessment of a subject's level of sedation.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCritical Illness
CountriesUnited States
CollaboratorsMedtronic - MITG
Timeline
N/ACompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartMay 2008
First PostedAug 2008
Primary CompletionApr 2011
Study CompletionJul 2011
TodayJul 2026
First PostedAug 14, 2008
Enrollment StartMay 1, 2008
Primary CompletionApr 1, 2011
Study CompletionJul 1, 2011
TodayJul 2, 2026
Enrollment to primary: 2.9 yearsPosted 17.9 years ago
Interventions
Bispectral Index (BIS) Monitordevice
BIS monitoring in addition to RASS assessments