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Ventricular Tachycardia (VT) Ablation or Escalated Drug Therapy

Ventricular Tachycardia Ablation or Escalated aNtiarrhythmic Drugs in ISchemic Heart Disease

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00905853
Acronym
VANISH
Enrollment
260
Registered
2009-05-21
Start date
2009-05-31
Completion date
2015-12-31
Last updated
2016-07-11

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

Conditions

Recurrent Ventricular Tachycardia

Keywords

Ventricular Tachycardia, Catheter Ablation, ICD therapy, Antiarrhythmic Drug Therapy, Ischemic Heart Disease

Brief summary

This study will compare aggressive antiarrhythmic therapy to catheter ablation for ventricular tachycardia in patients who have suffered prior myocardial infarction. The purpose of this study is to evaluate the optimal management of patients presenting with recurrent VT and receiving ICD therapy in spite of first-line antiarrhythmic drug therapy. The hypothesis is catheter ablation is superior to aggressive antiarrhythmic drug therapy for recurrent VT.

Detailed description

This is a multicentre, parallel group, two arm, unblinded, randomized clinical trial to compare two management strategies for patients with ischemic heart disease and recurrent ICD therapy despite at least one antiarrhythmic drug. The primary endpoint will be a composite of appropriate ICD shocks or death.

Interventions

PROCEDURECatheter Ablation

Intracardiac electrode catheters are placed via central vasculature to identify myocardial scar, and surviving conduction channels within the scar which form the substrate for ventricular tachycardia. Radiofrequency energy is applied to these sites, interrupting the VT circuits.

DRUGEscalated Antiarrhythmic Therapy

Patients who have 'failed' antiarrhythmic therapy (except amiodarone) will be prescribed: Amiodarone 400 mg twice daily for 2 weeks, followed by 400 mg/day for 4 weeks, followed by 200 mg/day thereafter. Patients who 'failed' amiodarone (less than 300mg/day) will be prescribed: Amiodarone 400 mg three times a day for 2 weeks, followed by 400 mg/day for 1 week and 300 mg/day thereafter. Patients who 'failed' amiodarone (greater or equal to 300mg/day) will be prescribed: Amiodarone at the current dose with the addition of mexiletine 400 to 800 mg/day

Sponsors

Abbott Medical Devices
CollaboratorINDUSTRY
Biosense Webster, Inc.
CollaboratorINDUSTRY
Canadian Institutes of Health Research (CIHR)
CollaboratorOTHER_GOV
John Sapp
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Prior Myocardial Infarction * An implantable defibrillator * One of the following VT events (within the past 3 months): * greater than or equal to 3 episodes of symptomatic VT treated with ATP * greater than or equal to 1 appropriate ICD shock * greater than or equal to 3 VT episodes within 24 hours * sustained VT below detection rate of the ICD documented by ECG * Failed first-line antiarrhythmic drug therapy as defined by one of: * Appropriate ICD therapy or sustained VT occurred while patient was taking amiodarone (stable dose \>/= 2 weeks) * Appropriate ICD therapy or sustained VT occurred on another antiarrhythmic drug (stable dose \>/= 2 weeks)

Exclusion criteria

* Active ischemia (acute thrombus, dynamic ST elevation on ECG) or another reversible cause of VT (eg. electrolyte abnormalities, drug induced arrhythmia) * Are known to be ineligible to take amiodarone (eg. active hepatitis, current hyperthyroidism, pulmonary fibrosis, known allergy) * Are ineligible for ablation (left ventricular thrombus, implanted mechanical aortic and mitral valves) * Renal Failure (creatinine clearance \< 15 ml/min) * Current NYHA functional class IV heart failure or CCS Functional Class IV angina * Recent ST elevation myocardial infarction (\< 1 month) * Recent coronary bypass surgery (\< 3 mon) or recent PCI (\< 1 mon) * Pregnant * prior ablation for ventricular tachycardia * A systemic illness likely to limit survival to \< 1 year * Unable or unwilling to provide informed consent

Design outcomes

Primary

MeasureTime frame
Appropriate ICD shocks,VT storm and death3 years

Secondary

MeasureTime frame
Appropriate ICD antitachycardia pacing anytime and after 1 month treatment period3 years
appropriate ICD shocks anytime and after 1 month treatment period3 years
Inappropriate shocks anytime and after 1 month treatment period3 years
VT storm anytime and after 1 month treatment period3 years
All cause mortality3 years
Number of ICD shocks3 years
Hospital admission for cardiac causes3 years
Procedural complications, amiodarone toxicity or adverse events3 years
Documented sustained VT below detection rate of the ICD any time and after 1 month treatment period3 years

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026