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Medical ANtiarrhythmic Treatment or Radiofrequency Ablation in Ischemic Ventricular Tachyarrhythmias

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

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02303639
Acronym
MANTRA-VT
Enrollment
120
Registered
2014-12-01
Start date
2015-04-30
Completion date
2018-06-30
Last updated
2016-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myocardial Infarction, Ventricular Tachyarrhythmia

Keywords

implantable cardioverter defibrillator, antiarrhythmic medication, catheter ablation

Brief 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.

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.

Interventions

PROCEDURERadiofrequency catheter ablation

Catheter ablation with an open-irrigated tip ablation catheter and 3D electroanatomical mapping

Amiodarone (or sotalol) for prevention of VT/VF relapses

Sponsors

Biosense Webster, Inc.
CollaboratorINDUSTRY
Central Finland Hospital District
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Number of ventricular tachycardia (VT) or ventricular fibrillation (VF) episodes12 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

MeasureTime frame
Cardiovascular mortality12 and 24 months
Time to first hospitalization and number of hospital days12 and 24 months
Comparative cost-effectiveness of the therapies12 and 24 months
Quality of life measured By SF-36 and EQ5D questionnaires12 and 24 months
Patient related outcome measured by the PHQ-9, GAD-7, ICDC-8 and EXPECT-ICD questionnaires12 and 24 months
Number of appropriate ICD therapies and sustained VT/VF episodes24 months
All cause mortality12 and 24 months
Number of electrical storm episodes12 and 24 months
Time to first VT/VFup to 24 months
Time to reablationup to 24 months
Number of inappropriate ICD therapiesup to 24 months
Number of atrial fibrillation and other supraventricular arrhythmia episodesup to 24 months
Number of non-sustained VT episodes12 and 24 months

Countries

Finland

Contacts

Primary ContactPekka Raatikainen, MD, PhD
pekka.raatikainen@ksshp.fi+358503169001

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026