Screening for delirium in the Intensive Care Unit: a comparison study

Screening for delirium in the Intensive Care Unit: a comparison study - screeningsinstruments for delirium IC

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON30770

Enrollment

100

Registered

2007-03-20

Start date

2007-02-15

Completion date

Unknown

Last updated

2024-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

acute confusion delirium

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: ICU-patients of the Univerity Medical Centre

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame
Primary study parameters are the diagnostic value of both screening instruments (sensitivity, specificity and predictive value) as compared to the gold standard, the DSM-IV criteria.	—

Secondary

Measure	Time frame
Secundary outcome parameters are the value of the impression of the ICU physician (sensitivity, specificity and predictive value) as compared to the gold standard, the DSM-IV criteria.	—

Countries

Netherlands

Outcome results