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Combining Objective and Subjective Sedation Assessment Tools

NCT00734409 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2013-03-29

Study results available
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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.

Conditions

  • Critical Illness

Interventions

DEVICE

Bispectral Index (BIS) Monitor

BIS monitoring in addition to RASS assessments

Sponsors & Collaborators

Principal Investigators

  • DaiWai M Olson, PhD RN · Duke University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-05-31
Primary Completion
2011-04-30
Completion
2011-07-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00734409 on ClinicalTrials.gov