Incidence of Delirium in Critically Ill Patients in a Dutch University Hospital
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|ClinicalTrials.gov Identifier: NCT00604773|
Recruitment Status : Completed
First Posted : January 30, 2008
Last Update Posted : August 31, 2010
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.
The primary aim is to determine the incidence of delirium and to determine risk factors for this group of patients to develop a prediction model.
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).
|Condition or disease|
|Study Type :||Observational|
|Estimated Enrollment :||700 participants|
|Official Title:||Incidence of Delirium in Critically Ill Patients in a Dutch University Hospital|
|Study Start Date :||February 2008|
|Actual Primary Completion Date :||February 2009|
|Actual Study Completion Date :||February 2009|
minimal one positive CAM-ICU score during ICU admission
without any positive CAM-ICU scores during ICU admission
- delirium [ Time Frame: during admission at the critical care ]
- markers of inflammation [ Time Frame: within 24 hours of delirium diagnosis ]
- biomarkers [ Time Frame: within 24 hours of delirium diagnosis ]
Biospecimen Retention: Samples With DNA
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00604773
|Radboud University Nijmegen Medical Centre, Critical Care|
|Nijmegen, Gelderland, Netherlands, 6500|
|Principal Investigator:||Hans vd Hoeven, MD, PhD||Radboud University|