I25.13
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Written authorization of the study participant - Age> 18 years - Coronary with or without cardiopulmonary bypass (CPB) - Type 2 diabetes and / or renal impairment (GFR = 35% and <70% and / or left ventricular ejection fraction of <= 35%
Exclusion criteria
Exclusion criteria: Lack of written consent - Pregnancy - aortic surgery - stenosis of the carotid artery > 70% - Documented dementia - state after stroke - Lack of knowledge of the German language - Lack of possibility of follow-up studies - Pacemakers or other electrical implants - Claustrophobia (Ban Reason for MR subanalysis) - Coronary (possible reason for exclusion of the MR sub-analysis). This will be decided on an individual basis according to the specifications of the stent manufacturer.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Statistically significantly lower postoperative deterioration of neurocognitive function compared with the control group Test methods used: - MoCA (Montreal Cognitive Assessment) - Rey-figure / figure Taylor - CVLT-k (California Verbal Learning Test - short) - TMT A and B - Boston Naming Test (BNT) -. Short form according Th Merten (2004) - Regensburger word liquid test (RWT) - Digit Span forward and backward - Block span | — |
Secondary
| Measure | Time frame |
|---|---|
| - Subclinical, morphological cerebrovascular events compared to baseline based MRI - Intraoperative measures to improve cerebral oxygenation - Duration of hospitalization - Duration intensive stay - Prevalence delirium - Biometric data and vital signs - Euro Core and Simplified Acute Physiology Score (SAPS) III - Hospital mortality | — |
Countries
Germany
Contacts
Universitätsklinik für Herz- und Thoraxchirurgie