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Clinical Trials/NCT00961389
NCT00961389
Unknown
Not Applicable

Validating a Delirium Prediction Model for Critically Ill Patients

Radboud University Medical Center1 site in 1 country650 target enrollmentMay 2009
ConditionsDelirium

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Delirium
Sponsor
Radboud University Medical Center
Enrollment
650
Locations
1
Primary Endpoint
delirium
Last Updated
16 years ago

Overview

Brief Summary

The objective of this study is to determine the incidence of delirium in adults patients who are admitted at the critical care unit of a Dutch University Hospital with the mapping of relevant delirium risk factors The primary aim is to validate the investigators' developed delirium prediction model for critical care patients.

A secondary aim is to find differences between delirious patients and non-delirious patients on different aspects of diagnostics, treatment and care, outcome, length of stay, and inflammation.

According to Dutch law, the need to obtain informed consent was waived by the Committee on Research Involving Human Subjects (CMO) of Nijmegen for this observational study (2007/283).

Registry
clinicaltrials.gov
Start Date
May 2009
End Date
October 2009
Last Updated
16 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • all adult patients (18 years and older) admitted at the critical care unit of our hospital

Exclusion Criteria

  • admitted \< 12 hours on ICU
  • not able to understand Dutch
  • patients with serious hearing and visibility disabilities
  • mentally retarded patients
  • patients suffering from receptive aphasia
  • delirious before admission

Outcomes

Primary Outcomes

delirium

Time Frame: during admission at the critical care

Secondary Outcomes

  • markers of inflammation(within 24 hours of delirium diagnosis)

Study Sites (1)

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