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

Critical Care Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00506649
• Other study ID #: 007
• Status: Completed
• Phase: N/A
• First received: July 23, 2007
• Last updated: July 23, 2007
• Start date: August 2003
• Est. completion date: November 2005

Study information

• Verified date: July 2007
• Source: Maisonneuve-Rosemont Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: Canada':'Ethics Review Committee'
• Study type: Observational

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1214
• Est. completion date: November 2005
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• All adult patients admitted to ICU

Exclusion Criteria:

• Repeat admission within the same hospitalisation; moribund patients

Study Design

Observational Model: Defined Population, Time Perspective: Longitudinal

Related Conditions & MeSH terms

• Critical Care

Intervention

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.

Locations

Country	Name	City	State
Canada	Hopital Maisonneuve Rosemont	Montreal	Quebec

Sponsors (1)

Lead Sponsor	Collaborator
Maisonneuve-Rosemont Hospital

Country where clinical trial is conducted

Canada,