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Validating a Delirium Prediction Model for Critically Ill Patients

R

Radboud University Medical Center

Status

Unknown

Conditions

Delirium

Study type

Observational

Funder types

Other

Identifiers

NCT00961389
2007/283-2

Details and patient eligibility

About

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).

Enrollment

650 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

650 participants in 2 patient groups

delirious patients
Description:
minimal any positive CAM-ICU score during ICU admission
non-delirious patients
Description:
without any positive CAM-ICU score during ICU admission

Trial contacts and locations

1

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Central trial contact

Mark van den Boogaard, MSc, R< CCRN; Peter Pickkers, MD, PhD

Data sourced from clinicaltrials.gov

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