Medical ANtiarrhythmic Treatment or Radiofrequency Ablation in Ischemic Ventricular Tachyarrhythmias

NCT02303639 — Phase 4, Unknown, 120 participants, Central Finland Hospital District

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Medical ANtiarrhythmic Treatment or Radiofrequency Ablation in Ischemic Ventricular Tachyarrhythmias. A Prospective, Randomized Multicentre Study.

RegistryNCT02303639, acronym MANTRA-VT
StatusUnknown
PhasePhase 4
Study typeInterventional; randomized, parallel, masking: none, treatment
Enrollment120 (Estimated)
SponsorCentral Finland Hospital District (Other); collaborators: Biosense Webster, Inc.
ConditionsMyocardial Infarction, Ventricular Tachyarrhythmia
InterventionsRadiofrequency catheter ablation, Antiarrhythmic drug therapy (Procedure, drug)
Datesstart 2015-04-01, primary completion 2017-06-01 (estimated), completion 2018-06-01 (estimated), first posted 2014-12-01, last updated 2016-09-01
Locations2 sites in Finland

Related Papers Related Patents Related Grants Related Experts
All trials for Myocardial Infarction All trials for Ventricular Tachyarrhythmia All trials of Radiofrequency catheter ablation All trials of Antiarrhythmic drug therapy

-Summary

The study evaluates whether catheter based radiofrequency ablation is superior to optimized antiarrhythmic medical therapy in preventing ventricular tachyarrhythmia relapses in patients with ischemic heart disease and implantable cardioverter defibrillator.

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+Detailed description

The study is designed to evaluate whether catheter based radiofrequency ablation is superior to optimized antiarrhythmic medical therapy in preventing ventricular tachyarrhythmia relapses among patients with prior myocardial infarction and implantable cardioverter defibrillator (ICD). The patients have not been using using chronic antiarrhythmic medication. Primary end point is number of ICD therapies (defibrillations, cardioversions and antitachycardia pacing) and otherwise documented sustained ventricular tachycardia (duration more than 30 s or hemodynamically unstable ) or ventricular fibrillation episodes during 12 months follow-up period. Secondary end points include mortality, hospitalization for cardiac reason, health economics, quality of life and several ICD and arrhythmia related issues. Total length of the follow-up is at least two years.

+Arms and interventions

ArmTypeInterventionsDescription
Radiofrequency catheter ablationExperimentalProcedure: Radiofrequency catheter ablationRadiofrequency catheter ablation using open-irrigated ablation catheter and 3D electroanatomical mapping
Antiarrhythmic drug therapyActive comparatorDrug: Antiarrhythmic drug therapyAmiodarone (or sotalol) tablet by mouth for the duration of the study
  • Radiofrequency catheter ablation (Procedure): Catheter ablation with an open-irrigated tip ablation catheter and 3D electroanatomical mapping
  • Antiarrhythmic drug therapy (Drug), also known as amiodarone, sotalol, class III antiarrhyhtmic agents: Amiodarone (or sotalol) for prevention of VT/VF relapses

+Outcome measures

Primary outcomes

  • Number of ventricular tachycardia (VT) or ventricular fibrillation (VF) episodes [12 months]: • Number of appropriate ICD therapies (defibrillation, cardioversion, antitachycardia pacing) for VT/VF and otherwise documented sustained VT or VF episodes at 12 months

Secondary outcomes

  • All cause mortality [12 and 24 months]
  • Cardiovascular mortality [12 and 24 months]
  • Time to first hospitalization and number of hospital days [12 and 24 months]
  • Comparative cost-effectiveness of the therapies [12 and 24 months]
  • Quality of life measured By SF-36 and EQ5D questionnaires [12 and 24 months]
  • Patient related outcome measured by the PHQ-9, GAD-7, ICDC-8 and EXPECT-ICD questionnaires [12 and 24 months]
  • Number of appropriate ICD therapies and sustained VT/VF episodes [24 months]
  • Number of non-sustained VT episodes [12 and 24 months]
  • Number of electrical storm episodes [12 and 24 months]
  • Time to first VT/VF [up to 24 months]
  • Time to reablation [up to 24 months]
  • Number of inappropriate ICD therapies [up to 24 months]
  • Number of atrial fibrillation and other supraventricular arrhythmia episodes [up to 24 months]

+Eligibility

Sex: All, ages: 18 Years to 80 Years

Inclusion Criteria:

* Patients 18-80 years of age with prior myocardial infarction and ICD (single chamber, dual chamber ICD or ICD with biventricular pacing capability (CRT-D)) for primary or secondary prevention of sudden cardiac death (SCD), who have had at least two documented episodes of sustained VT or VF and no chronic amiodarone treatment for ventricular tachyarrhythmias

Exclusion Criteria:

* Age less than 18 years or more than 80 years
* Non-ischemic cardiomyopathy
* Ongoing chronic treatment of ventricular tachyarrhythmias with amiodarone, intolerance/contraindication to all class III antiarrhythmic drugs (i.e., intolerance/contraindication to one class III agents is not excluding the patient if another one can be used)
* Contraindication to endocardial catheter ablation (e.g., intracavitary thrombi, contraindication to perioperative anticoagulation)
* Previous VT/VF ablation
* Open heart surgery within 3 months
* Prosthetic heart valve
* Planned revascularization (PCI or CABG)
* Surgery for structural heart disease or heart transplantation
* Pregnancy or planned pregnancy within the follow-up period
* Secondary cause for VT/VF (e.g., acute myocardial infarction)
* Patient does not want to participate
* Life expectancy less than 12 months

+Locations (2)

FacilityCityCountryStatus
Central Finland Central HospitalJyväskyläFinlandRecruiting
Heart Center Tampere University HospitalTampereFinlandRecruiting

+Investigators