Evaluation of Intraoperative Dexmedetomidine Use in Patients Undergoing Surgical Aortic Valve Replacement
Systemic Inflammatory Response, Aortic Valve Stenosis
About this trial
This is an interventional treatment trial for Systemic Inflammatory Response focused on measuring dexmedetomidine
Eligibility Criteria
Inclusion Criteria: isolated aortic stenosis adult patients with written consent Exclusion Criteria: BMI <30kg/m2 1st, 2nd and 3rd degree AV block bradycardia HR<50/min upon arrival to operating theatre neurological disorders (Parkinson's disease, Myasthenia gravis, multiple sclerosis, brain tumors in anamnesis) recent use of psychoactive drugs alcohol and illicit drug addiction diabetes type I with complications patients who develop hypotension after initiation of dexmedetomidine infusion requiring vasoconstriction therapy patients receiving corticosteroids in perioperative period patients with known allergy to dexmedetomidine
Sites / Locations
- University hospital DubravaRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Placebo Comparator
Experimental
Experimental
Saline
Dexmedetomidine 0.5
Dexmedetomidine 1
Continuous infusion of saline starting after invasive monitoring placement and before initiation of cardiopulmonary bypass (CPB) until the end of surgery
Continuous infusion of dexmedetomidine in dose 0.5 mcg/kg/min starting after invasive monitoring placement and before initiation of cardiopulmonary bypass (CPB) until the end of surgery
Continuous infusion of dexmedetomidine in dose 1 mcg/kg/min starting after invasive monitoring placement and before initiation of cardiopulmonary bypass (CPB) until the end of surgery