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

NCT00506649 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1214

Last updated 2007-07-25

No results posted yet for this study

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.

Conditions

  • Critical Care

Interventions

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.

Sponsors & Collaborators

  • Maisonneuve-Rosemont Hospital

    lead OTHER

Principal Investigators

  • Yoanna Skrobik, MD FRCP(c) · Maisonneuve-Rosemont Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-08-31
Completion
2005-11-30

Countries

  • Canada

Study Locations

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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 NCT00506649 on ClinicalTrials.gov