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Clinical Trials/NCT00506649
NCT00506649CompletedNot Applicable

Comparison of no Protocol vs Protocolized Approach to Pain, Sedation and Delirium Management in the ICU

Maisonneuve-Rosemont Hospital1 site in 1 country1,214 target enrollmentStarted: August 2003Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
1,214
Locations
1
Study OverviewStudy DesignEligibility CriteriaInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

To assess pain, agitation, and delirium experienced by critically ill patients daily and evaluate the impact of a protocol; to compare the incidence of coma and delirium, length of stay, mortality and costs of care between pre- and post-protocol groups.

Study Design

Study Type
Observational
Observational Model
Defined Population
Time Perspective
Other

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •All adult patients admitted to ICU

Exclusion Criteria

  • •Repeat admission within the same hospitalisation; moribund patients

Investigators

Sponsor Class
Other

Study Sites (1)

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