The primary objective of the study is to check the ability of Neurokeeper's algorithm system to detect and monitor changes in cerebral electrophysiological parameters as compared to clinical evaluation in patients undergoing cardiac surgery.
The secondary objectives is correlations of EEG + ERP measurements with clinical evaluations as assessed by NIHSS ThiS study is a prospective, open label, single arm, self control, single center study.
This study will be conducted in 50 subjects according to the inclusions/exclusions criteria.
- Neurokeeper stroke detector Device
Intervention Desc: Electrophisoloigcal monitoring ARM 1: Kind: Experimental Label: Patients undergoing cardiac surgery
- Observation: Cohort
- Perspective: Prospective
- Sampling: Non-Probability Sample
Patients undergoing cardiac surgery.
|Type||Measure||Time Frame||Safety Issue|
|Primary||Neurological detrioration detection||No|
|Secondary||Time from deterioration to detection||No|