Recruitment

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