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INTERVENE: Indian Trial of Endocardial Ventricular Substrate Ablation to Prevent Recurrent VT Events

INTERVENE: Indian Trial of Endocardial Ventricular Substrate Ablation to Prevent Recurrent VT Events

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02301390
Acronym
INTERVENE
Enrollment
53
Registered
2014-11-25
Start date
2009-10-31
Completion date
2016-09-30
Last updated
2020-01-27

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

Conditions

Ventricular Tachycardia

Keywords

INTERVENE, Ventricular tachycardia, India

Brief summary

This study to is being conducted in India to determine the role of catheter-based ablation for ventricular tachycardia (VT) in post- heart attack patients who meet established guidelines for implantable cardiodefibrillator (ICD) implantation, but cannot afford it. These patients would be started on chronic Amiodarone therapy, which has been shown to be effective but can often lead to multiple side effects. Patients will therefore be randomized in an even proportion to either a) the control group, receiving chronic Amiodarone therapy, or the study group, undergoing catheter ablation of VT in addition to chronic Amiodarone therapy. This trial will serve as a representative model for the developing world.

Detailed description

Sudden cardiac death (SCD) accounts for approximately 50% of all cardiac death, representing an estimated annual incidence ranging from 250,000 to 350,000 cases in the United States. The pathophysiologic mechanism for sudden death in the majority of these patients is thought to be ventricular tachycardia (VT) related to coronary artery disease (CAD), which can then degenerate to ventricular fibrillation (VF). Patients who survive an initial episode of VT/VF are prone to an extremely high incidence of recurrent life-threatening events (\ 25% at one year). Even in patients without a history of VT/VF, the presence of CAD and left ventricular (LV) dysfunction confers a two-year mortality rate of 22%. If VT is inducible at electrophysiological testing, the two-year mortality is \ 30%. The pathogenesis of VT in the setting of CAD is reentry in the area of the scarred myocardium. After an MI, the tissue can be broadly divided into three zones: the dense scar, the surrounding live myocardial tissue, and the intervening border zone. After a myocardial infarction (MI), the border zone between dense scar and live tissue contains electrically-active live myocardial fibrils interspersed in areas of infarcted, fibrotic tissue-setting the stage for local reentrant circuits that result in VT. The use of antiarrhythmic medications (AADs) to suppress the occurrence/recurrence of VT/VF in these high-risk patients has been mostly disappointing. In large clinical trials, most AADs have not only proved to be inefficacious, but to actually increase mortality. The one potential exception appears to be Amiodarone: one study suggests some mortality benefit (GESICA), while others suggest that Amiodarone provides significant antiarrhythmic benefits without a change in mortality (EMIAT, CAMIAT, SCD-HeFT). However, even the use of Amiodarone is plagued with multiple organ toxicities, ranging from pulmonary fibrosis to hepatitis, and thyroid dysfunction. An important alternative to such questionably efficacious antiarrhythmics is the implantable cardio-defibrillator (ICD), which can accurately and effectively detect and terminate VT/VF, resulting in a significant mortality benefit in both the primary and secondary prevention of sudden cardiac death. Yet, despite these beneficial results, ICD implantation cannot be considered a cure for VT. In addition, it is common for patients to experience painful high-voltage shocks secondary to recurrent ventricular arrhythmias, or to lose consciousness prior to the delivery of therapy. Moreover, the considerable cost of ICDs severely limits their availability in the developing world-where public and/or private health insurance systems are rudimentary at best, and where the incidence of coronary artery disease is four times higher than that of the developed world-highlighting the urgency of establishing an alternative therapy for post-MI patients with ventricular arrhythmias that is both accessibly and effective. One such option may be catheter ablation of ventricular arrhythmias. It has been well described that for hemodynamically-stable VT circuits, careful ventricular mapping to identify sites critical to the maintenance of a given circuit, followed by discrete applications of catheter-based radiofrequency (RF) energy, can effectively eliminate VT. This strategy mocks surgical approaches that have been used extensively since the late 1970s for modification of the arrhythmogenic substrate in patients with chronic myocardial infarction. Since the location of the reentrant circuit is most often located at the junction of the normal and scarred myocardium, two effective general strategies were developed over time: a) subendocardial resection-involving surgical removal of the subendocardial layer containing the arrhythmogenic substrate in this border zone, and b) encircling endocardial ventriculotomy-consisting of the placement of a circumferential surgical lesion through the border zone and, presumably, interrupting potential VT circuits. When performed at experienced centers, the long-term freedom from malignant VT/VF after surgery is \>90%. However, the significant mortality (3-14%) and morbidity associated with this invasive procedure has curtailed its use in general practice. The less invasive, catheter approach to substrate modification relies on electroanatomical mapping systems that create a high fidelity representation of the endocardium, allowing for the reconstruction and electronic manipulation of an endocardial cast of the ventricular chamber that carefully delineates the normal and abnormal tissues. This is based on the observation that during normal sinus rhythm, there are distinguishing characteristics of the endocardial electrogram (EGM) of normal and abnormal tissue: abnormal tissue manifests lower voltage amplitude, prolonged EGM duration, and the presence of late and fractionated potentials. Marchlinski and colleagues reported in a seminal study that by using a substrate-mapping strategy, catheter-based RF ablation lesions directed in a linear fashion were effective in controlling scar-related drug-refractory unstable VT. Furthermore, using this high-density electroanatomical mapping 1) this strategy can be utilized to localize the arrhythmogenic substrate in the majority of patients with a history of myocardial infarction and sustained ventricular tachyarrhythmia's, and 2) RF ablation using an irrigated-tip ablation catheter can be effectively and safely used to modify the arrhythmogenic substrate to render VT non-inducible even in the presence of multiple VT morphologies. The favorable results in these non-randomized reports prompted the initiation of SMASH-VT (Substrate Mapping & Ablation in Sinus Rhythm to Halt Ventricular Tachycardia Trial); a prospective randomized clinical trial to objectively assess the clinical utility of substrate ablation of scar-related VT. This trial was a randomized-controlled trial examining the role of substrate mapping and RF ablation in the primary prevention of ICD shocks in patients presenting with clinically life-threatening VT/VF. That is, patients with a history of MI, and who survive an episode of VT/VF are at high-risk for recurrent VT and thus treated with ICDs (in essence, these patients meet AVID/CIDS/CASH criteria). In normal clinical practice, these patients are not routinely treated with adjuvant medications because of their proarrhythmic potential and side effects. In addition to an ICD and routine clinical care, these patients were additionally randomized in SMASH-VT to substrate-based catheter ablation. This catheter ablation group underwent electroanatomic mapping to delineate the endocardial infarct margins (CARTO, Biosense-Webster, Inc.). Substrate modification was then performed targeting the exit sites of induced VTs and/or late potentials within the scar using standard or irrigated radiofrequency ablation catheters. As published in late 2007 (Reddy et al, NEJM, 357:2657), the 30-day post-ablation mortality was zero, and there was no significant change in ventricular function or functional class during follow up. During an average follow-up of 22.5±5.5 months, appropriate defibrillator therapy (anti-tachycardia pacing and shocks) occurred in 21 control (33%) and 8 ablation (12%) patients (p=0.007 by the log rank test). Of these, appropriate defibrillator shocks alone occurred in 20 control (31%) and 6 ablation (9%) patients (p=0.003). Mortality was not increased in the ablation arm (control 17%, ablation 9%; p=0.29); indeed, there was a trend to decreased mortality in the ablation arm. Thus, the SMASH-VT study revealed several important points: 1) adjuvant substrate based catheter ablation is feasible in this patient population, 2) use of a saline-irrigated RF ablation catheter for this ablation strategy is safe, and 3) this strategy decreases subsequent ICD therapies in post-myocardial infarction patients receiving defibrillators for the secondary prevention of sudden death. The favorable results of SMASH-VT, combined with considerable technical and scientific improvements in catheter ablation of scar-related VT, also raise the possibility that the therapeutic benefit of ablation may be extrapolated to similar patients in the developing world, who have had an MI and have survived a ventricular arrhythmic event, but are unable to afford an ICD. This is of particular importance because such patients are typically treated with chronic Amiodarone therapy-a strategy with an unestablished mortality benefit and significant side effects. The investigators therefore propose a randomized clinical trial, in which India-a nation with a population of 1.2 billion-will serve as a representative model for the developing world. The study will evaluate the safety and efficacy of adjunctive catheter ablation in post-myocardial infarction patients who have additionally survived a ventricular arrhythmic event, and would be initiated on chronic Amiodarone therapy because of an inability to afford ICD therapy. Patients will therefore be randomized in an even proportion to either a) the control group, receiving chronic Amiodarone therapy, or the study group, undergoing catheter ablation of VT in addition to chronic Amiodarone therapy.

Interventions

DRUGAmiodarone

Amiodarone is a Class III antiarrhythmic agent.

DEVICECatheter Ablation

The ablation procedure uses radiofrequency energy to destroy cardiac tissue at the origin of the arrhythmia.

Sponsors

Biosense Webster, Inc.
CollaboratorINDUSTRY
Icahn School of Medicine at Mount Sinai
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* ≥ 18 and ≤ 85 years of age * History of a remote MI (≥1 month) * Survival of a ventricular arrhythmic event (VT/VF) that would mandate placement of an implantable cardioverter-defibrillator (ICD) (Patients who experience a ventricular arrhythmic event (VT/VF) while already being treated with Amiodarone (100-200 mg/day) are not excluded from the study. This is permitted provided that the patient had been treated with Amiodarone for at least 2 months prior to experiencing the index VT/VF event. These patients are randomized to either a higher dose of Amiodarone (e.g., 100mg/day -\> 200mg/day or 200mg/day -\> 400mg/day) or a higher dose of Amiodarone plus catheter ablation.) * Patient cannot afford an ICD and thus has been planned for treatment with Amiodarone (or an increased dose of Amiodarone) * Ability to understand the requirements of the study * Willingness to adhere to study restrictions and comply with all post- procedural follow-up requirements

Exclusion criteria

* Patients with NYHA class IV congestive heart failure * Prior ablation for a ventricular arrhythmia * Presence of an LV thrombus * Contraindication to anticoagulation * Inability to access the endocardium because of mechanical mitral and aortic valve * Life expectance \<1 year for any medical condition

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants Who Were Free From All-cause Mortality, Sustained VT or Cardiac Arrestat 24 monthsNumber of participants who had no occurrences of all-cause mortality, sustained ventricular tachycardia (VT) and cardiac arrest at 24 months

Secondary

MeasureTime frameDescription
Number of Participant Who Diedup to 24 monthsNumber of subjects that die within 30 days or die by 24 months.
Ventricular Arrhythmic Eventsat 24 monthsTotal number of ventricular arrhythmic events, compared between the 2 treatment arms.
Change in LV Ejection Fractionbaseline and 24 monthsChange in left ventricle (LV) ejection fraction between paired measurements recorded at 24 months as compared to baseline

Countries

India

Participant flow

Participants by arm

ArmCount
Amiodarone Only
Amiodarone is a Class III antiarrhythmic agent.
27
Amiodarone + Catheter Ablation
Amiodarone is a Class III antiarrhythmic agent. Catheter VT Ablation: The ablation procedure uses radiofrequency energy to destroy cardiac tissue at the origin of the arrhythmia.
26
Total53

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyDeath22
Overall StudyLost to Follow-up01
Overall StudyMissed multiple visits11
Overall StudyPhysician Decision10
Overall StudyProcedure not completed04
Overall StudyProtocol Violation10
Overall Studystudy terminated20
Overall StudyWithdrawal by Subject35

Baseline characteristics

CharacteristicAmiodarone + Catheter AblationTotalAmiodarone Only
Age, Continuous53.8 years
STANDARD_DEVIATION 10.4
54.3 years
STANDARD_DEVIATION 10.5
54.9 years
STANDARD_DEVIATION 10.7
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants0 Participants0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
26 Participants53 Participants27 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
26 Participants53 Participants27 Participants
Race (NIH/OMB)
Black or African American
0 Participants0 Participants0 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
0 Participants0 Participants0 Participants
Sex: Female, Male
Female
2 Participants3 Participants1 Participants
Sex: Female, Male
Male
24 Participants50 Participants26 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
2 / 272 / 26
other
Total, other adverse events
4 / 276 / 26
serious
Total, serious adverse events
11 / 278 / 26

Outcome results

Primary

Number of Participants Who Were Free From All-cause Mortality, Sustained VT or Cardiac Arrest

Number of participants who had no occurrences of all-cause mortality, sustained ventricular tachycardia (VT) and cardiac arrest at 24 months

Time frame: at 24 months

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Amiodarone OnlyNumber of Participants Who Were Free From All-cause Mortality, Sustained VT or Cardiac Arrest16 Participants
Amiodarone + Catheter AblationNumber of Participants Who Were Free From All-cause Mortality, Sustained VT or Cardiac Arrest21 Participants
Secondary

Change in LV Ejection Fraction

Change in left ventricle (LV) ejection fraction between paired measurements recorded at 24 months as compared to baseline

Time frame: baseline and 24 months

Population: Data for only those who had two time points LV ejection fraction data

ArmMeasureValue (MEAN)Dispersion
Amiodarone OnlyChange in LV Ejection Fraction1.85 percentStandard Deviation 6.32
Amiodarone + Catheter AblationChange in LV Ejection Fraction8 percentStandard Deviation 0.31
Secondary

Number of Participant Who Died

Number of subjects that die within 30 days or die by 24 months.

Time frame: up to 24 months

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
Amiodarone OnlyNumber of Participant Who Diedwithin 30 days0 Participants
Amiodarone OnlyNumber of Participant Who Died24 months2 Participants
Amiodarone + Catheter AblationNumber of Participant Who Diedwithin 30 days0 Participants
Amiodarone + Catheter AblationNumber of Participant Who Died24 months2 Participants
Secondary

Ventricular Arrhythmic Events

Total number of ventricular arrhythmic events, compared between the 2 treatment arms.

Time frame: at 24 months

ArmMeasureValue (NUMBER)
Amiodarone OnlyVentricular Arrhythmic Events15 events
Amiodarone + Catheter AblationVentricular Arrhythmic Events5 events

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026