Propafenone Versus Amiodarone in Septic Shock (PRASE)
Supraventricular Arrhythmia, Septic Shock
About this trial
This is an interventional treatment trial for Supraventricular Arrhythmia focused on measuring Supraventricular Arrhythmia, Septic shock, Propafenone, Amiodarone, Intensive Care
Eligibility Criteria
Inclusion Criteria:
- Septic shock with a new onset SV arrhythmia
- LV systolic function normal to moderately reduced according to echocardiography.
Exclusion Criteria:
- Severe LV systolic dysfunction
- More than 1st degree AV block
- High dose vasopressor therapy with continuous noradrenaline > 1.0 ug/kg.min
- Known intolerance to amiodarone or propafenone
- Absence of septic shock
- Chronic AF
- Dependence on pacemaker
- Status after MAZE procedure
Sites / Locations
- Dept. Anaesthesia and Intensive Care, 3rd Medical Faculty, Charles University
- Dept of Anaesthesia and Intensive Care, General University Hospital, 1st Medical Faculty, Charles University
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Propafenone i.v.
Amiodarone i.v.
Patients in septic shock with a new onset supraventricular arrhythmia are randomized either to arm treated with propafenone or with amiodarone. Both arms will have standard treatment, there are no limits to indicated electric cardioversion as part of treatment. Intervention: Bolus of 35-70 mg intravenous propafenone followed by continuous infusion of 400-840 mg/24h.
Patients in septic shock with a new onset supraventricular arrhythmia are randomized either to arm treated with propafenone or with amiodarone. Both arms will have standard treatment, there are no limits to indicated electric cardioversion as part of treatment. Intervention: Bolus of 150-300 mg of intravenous amiodarone followed by continuous infusion of 600-1800 mg/24h.