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Validation of the Confusion Assessment Method for Intermediate Care Units (CAM-IMC)

Validation of the Confusion Assessment Method for Intermediate Care Units (CAM-IMC) - CAM-IMC validation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00026980
Enrollment
156
Registered
2021-10-25
Start date
2021-11-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

F05.8

Interventions

Group 1: Patients with preoperatively assessed for cognitive impairment and for postoperative delirium after surgery. Postoperative assessments will be performed with the delirium assessment tool to b

Sponsors

Universitätsklinik für Anästhesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: Informed consent

Exclusion criteria

Exclusion criteria: Brain pathologies leading to being unable to assess cognitive dysfunctions, such as dementia and stroke, age < 50 years, decline to consent, insufficient language skills preventing cognitive tests.

Design outcomes

Primary

MeasureTime frame
Prevalence of delirium on day 1, day 2 or day 3 after surgery.

Secondary

MeasureTime frame
Comparison of delirium assessment of the CAM-IMC with reference rater on day 1, day 2 and day 3 after surgery.

Countries

Germany

Contacts

Public ContactUlf Günther

Univeristätsklinik für Anästhesiologie, Intensivmedizin, Notfallmedizin, SchmerztherapieKlinikum Oldenburg

anaesthesie@klinkum-oldenburg.de04414032541

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 6, 2026