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Aortic atheroma burden and cognitive dysfunction after cardiac surgery

Aortic atheroma burden and cognitive dysfunction after cardiac surgery - POCD

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON30070
Enrollment
250
Registered
2006-10-19
Start date
2006-09-01
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

Atherosclerosis

Interventions

None listed

Sponsors

Isala Klinieken
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: A sub-sample of patients included in the diagnostic trial A-view: *Diagnostic value of an innovative non-invasive diagnostic to determine the grade of atherosclerosis before sternotomy in patients scheduled for cardiac surgery*. Patients over 65 years, undergoing sternotomy for elective cardiac surgery will be included in this study.

Exclusion criteria

Exclusion criteria: Patients who undergo a re-operation or off-pump surgery, suffer from neurodegenerative disease or a known psychiatric disorder and patients who are thought to be inable to perform neurocognitive testing will be excluded from participation in the subsample.

Design outcomes

Secondary

MeasureTime frame
The relation between atherosclerosis of the ascending aorta and neurocognitive function at discharge, stroke, transient ischemic attack, myocardial infarction and renal failure.

Primary

MeasureTime frame
Primary: The relation between atherosclerosis of the ascending aorta and neurocognitive function at three months after surgery.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)