I25.0 I08.3
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: -planned and elective cardiac surgery with or without CPB - Age >18 years - Written informed consent
Exclusion criteria
Exclusion criteria: - Patient refusal - Allocation to concurrent interventional trials - Clinical staff or relatives - Special operative procedures in hypothermia (i.e. aortic arch operation) - Conceivable CPB time >3h - In case of unforeseeable CBP time >3h or massive intraoperative bleeding, patients will be excluded for final study analysis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the impact of EEG processed neuromonitoring on intraoperative vasopressor support. Primary endpoint: cumulative intraoperative vasopressor application | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints focus on (1) intraopoerative fluid administration, (2) intraoperative awareness, (3) time to extubation after surgery, (4) postoperative confusedness and (5) sleep depth between the study arm and control patients | — |
Countries
Germany
Contacts
Klinik für Anästhesiologie und IntensivmedizinUniversitätsklinikum Jena