NCT00506649

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,214

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Aug 2003

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2003

Completed
2.3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2005

Completed
1.7 years until next milestone

First Submitted

Initial submission to the registry

July 23, 2007

Completed
2 days until next milestone

First Posted

Study publicly available on registry

July 25, 2007

Completed
Last Updated

July 25, 2007

Status Verified

July 1, 2007

First QC Date

July 23, 2007

Last Update Submit

July 23, 2007

Conditions

Critical Care

Keywords

protocolanalgesiasedationdeliriumcoma

Interventions

protocolOTHER

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.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • All adult patients admitted to ICU

You may not qualify if:

  • Repeat admission within the same hospitalisation; moribund patients

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hopital Maisonneuve Rosemont

Montreal, Quebec, H1T 2M4, Canada

Location

MeSH Terms

Conditions

AgnosiaDeliriumComa

Interventions

Clinical Protocols

Condition Hierarchy (Ancestors)

Perceptual DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and SymptomsConfusionNeurocognitive DisordersMental DisordersUnconsciousnessConsciousness Disorders

Intervention Hierarchy (Ancestors)

TherapeuticsEpidemiologic Study CharacteristicsHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and Evaluation

Study Officials

  • Yoanna Skrobik, MD FRCP(c)

    Maisonneuve-Rosemont Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
DEFINED POPULATION
Time Perspective
OTHER
Sponsor Type
OTHER

Study Record Dates

First Submitted

July 23, 2007

First Posted

July 25, 2007

Study Start

August 1, 2003

Study Completion

November 1, 2005

Last Updated

July 25, 2007

Record last verified: 2007-07

Locations

CA(1)