Propafenone Versus Amiodarone in Septic Shock
Last updated on July 2021Recruitment
- Recruitment Status
- Recruiting
- Estimated Enrollment
- 100
Summary
- Conditions
- Septic Shock
- Supraventricular Arrhythmia
- Type
- Interventional
- Phase
- Phase 4
- Design
- Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Single (Investigator)Masking Description: Provided by a dedicated study nursePrimary Purpose: Treatment
Participation Requirements
- Age
- Between 16 years and 90 years
- Gender
- Both males and females
Description
Primary aim is to verify the conclusions of the retrospective study, i.e. efficacy and safety of propafenone, in a prospective blinded randomized trial performed in two large intensive care units. Secondary aims are to monitor the electromechanics of left atrium in patients with SV arrhythmias in se...
Primary aim is to verify the conclusions of the retrospective study, i.e. efficacy and safety of propafenone, in a prospective blinded randomized trial performed in two large intensive care units. Secondary aims are to monitor the electromechanics of left atrium in patients with SV arrhythmias in septic shock.
Tracking Information
- NCT #
- NCT03029169
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: Martin Balik, A/Prof Dept of Anaesthesia and Intensive Care