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Propafenone Versus Amiodarone in Septic Shock (PRASE)

Primary Purpose

Supraventricular Arrhythmia, Septic Shock

Status
Completed
Phase
Phase 4
Locations
Czechia
Study Type
Interventional
Intervention
Propafenone i.v.
Amiodarone i.v.
Sponsored by
Charles University, Czech Republic
About
Eligibility
Locations
Arms
Outcomes
Full info

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

16 Years - 90 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Active Comparator

Active Comparator

Arm Label

Propafenone i.v.

Amiodarone i.v.

Arm Description

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.

Outcomes

Primary Outcome Measures

Efficacy of propafenone
cardioversion rate
ICU mortality of septic shock patients on propafenone for a SV arrhythmia
ICU mortality
28-day mortality of septic shock patients on propafenone for a SV arrhythmia
28-day mortality
12-month mortality of septic shock patients on propafenone for a SV arrhythmia
12-month mortality

Secondary Outcome Measures

Electromechanics of left atrium
left atrial emptying
Electromechanics of LA
isovolumic and ejection times

Full Information

First Posted
December 7, 2016
Last Updated
August 1, 2022
Sponsor
Charles University, Czech Republic
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1. Study Identification

Unique Protocol Identification Number
NCT03029169
Brief Title
Propafenone Versus Amiodarone in Septic Shock
Acronym
PRASE
Official Title
Prospective Randomized Study of Efficacy and Safety of 1c Class Antiarrhythmic Agent (Propafenone) in Septic Shock
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
October 23, 2017 (Actual)
Primary Completion Date
July 4, 2022 (Actual)
Study Completion Date
August 1, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Charles University, Czech Republic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Arrhythmias accompany septic shock in increased rates than in other ICU cohorts and their presence and management are related to patient´s prognosis. 1c class antiarrhythmics are seldom administered in intensive care due to a dose dependent toxicity published in case reports and unfavourable outcome reported in a few prospective trials done on cardiology patients. The papers on 1c class antiarrhythmics do not take into consideration a complex haemodynamic assessment using echocardiography. The authors have recently presented a retrospective study on SV arrhythmias in septic shock patients demonstrating favourable effect and safety of propafenone which showed higher antiarrhythmic efficacy than amiodarone.
Detailed 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 septic shock.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Supraventricular Arrhythmia, Septic Shock
Keywords
Supraventricular Arrhythmia, Septic shock, Propafenone, Amiodarone, Intensive Care

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Investigator
Masking Description
Provided by a dedicated study nurse
Allocation
Randomized
Enrollment
210 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Propafenone i.v.
Arm Type
Active Comparator
Arm Description
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.
Arm Title
Amiodarone i.v.
Arm Type
Active Comparator
Arm Description
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.
Intervention Type
Drug
Intervention Name(s)
Propafenone i.v.
Other Intervention Name(s)
Antiarrhythmic therapy
Intervention Description
Treatment
Intervention Type
Drug
Intervention Name(s)
Amiodarone i.v.
Other Intervention Name(s)
Antiarrhythmic therapy
Intervention Description
Treatment
Primary Outcome Measure Information:
Title
Efficacy of propafenone
Description
cardioversion rate
Time Frame
1 year
Title
ICU mortality of septic shock patients on propafenone for a SV arrhythmia
Description
ICU mortality
Time Frame
1 year
Title
28-day mortality of septic shock patients on propafenone for a SV arrhythmia
Description
28-day mortality
Time Frame
2 years
Title
12-month mortality of septic shock patients on propafenone for a SV arrhythmia
Description
12-month mortality
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Electromechanics of left atrium
Description
left atrial emptying
Time Frame
1 year
Title
Electromechanics of LA
Description
isovolumic and ejection times
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Martin Balik, A/Prof
Organizational Affiliation
Dept of Anaesthesia and Intensive Care
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dept. Anaesthesia and Intensive Care, 3rd Medical Faculty, Charles University
City
Prague 10
ZIP/Postal Code
100 34
Country
Czechia
Facility Name
Dept of Anaesthesia and Intensive Care, General University Hospital, 1st Medical Faculty, Charles University
City
Prague 2
ZIP/Postal Code
128 08
Country
Czechia

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31481571
Citation
Balik M, Waldauf P, Maly M, Matousek V, Brozek T, Rulisek J, Porizka M, Sachl R, Otahal M, Brestovansky P, Svobodova E, Flaksa M, Stach Z, Pazout J, Duska F, Smid O, Stritesky M. Efficacy and safety of 1C class antiarrhythmic agent (propafenone) for supraventricular arrhythmias in septic shock compared to amiodarone: protocol of a prospective randomised double-blind study. BMJ Open. 2019 Sep 3;9(9):e031678. doi: 10.1136/bmjopen-2019-031678.
Results Reference
derived

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Propafenone Versus Amiodarone in Septic Shock

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