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Improved ICU Outcomes With Protocolized Management of Analgesia, Sedation and Delirium

This study has been completed.
Sponsor:
Information provided by:
Maisonneuve-Rosemont Hospital
ClinicalTrials.gov Identifier:
NCT00506649
First received: July 23, 2007
Last updated: NA
Last verified: July 2007
History: No changes posted

July 23, 2007
July 23, 2007
August 2003
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No Changes Posted
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Improved ICU Outcomes With Protocolized Management of Analgesia, Sedation and Delirium
Comparison of no Protocol vs Protocolized Approach to Pain, Sedation and Delirium Management in the ICU

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.

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Observational
Observational Model: Defined Population
Time Perspective: Longitudinal
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Critical Care
Other: protocol
management protocols of non-pharmacological strategies and individualized titration of analgesics, sedatives, and anti-psychotics based on observed scores to manage sedation, analgesia and delirium.
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
1214
November 2005
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Inclusion Criteria:

  • All adult patients admitted to ICU

Exclusion Criteria:

  • Repeat admission within the same hospitalisation; moribund patients
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Canada
 
NCT00506649
007
No
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Maisonneuve-Rosemont Hospital
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Principal Investigator: Yoanna Skrobik, MD FRCP(c) Maisonneuve-Rosemont Hospital
Maisonneuve-Rosemont Hospital
July 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP