Improved ICU Outcomes With Protocolized Management of Analgesia, Sedation and Delirium
Completed
- Conditions
- Critical Care
- Registration Number
- NCT00506649
- Lead Sponsor
- Maisonneuve-Rosemont Hospital
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 1214
Inclusion Criteria
- All adult patients admitted to ICU
Exclusion Criteria
- Repeat admission within the same hospitalisation; moribund patients
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Hopital Maisonneuve Rosemont
🇨🇦Montreal, Quebec, Canada