Screening for delirium in the Intensive Care Unit: a comparison study
Completed
- Conditions
- acute confusiondelirium10012221
- Registration Number
- NL-OMON30770
- Lead Sponsor
- niversitair Medisch Centrum Utrecht
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
ICU-patients of the Univerity Medical Centre
Exclusion Criteria
Patient who are deeply sedated ( Ramsayscore 5 or 6 )
Comatose patients (Glasgow Coma Score less than 8)
Patients who receive sedatives between evaluations with the various instruments
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Primary study parameters are the diagnostic value of both screening<br /><br>instruments (sensitivity, specificity and predictive value) as compared to the<br /><br>gold standard, the DSM-IV criteria.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Secundary outcome parameters are the value of the impression of the ICU<br /><br>physician (sensitivity, specificity and predictive value) as compared to the<br /><br>gold standard, the DSM-IV criteria.</p><br>
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie delirium in ICU patients with acute confusion?
How does the delirium screening tool in NL-OMON30770 compare to standard-of-care assessments in ICU settings?
Are there specific biomarkers that correlate with delirium severity in critical care patients?
What are the most effective management strategies for ICU delirium-related adverse events?
What are the current drug targets being explored for delirium prevention in critical care medicine?