Ventricular Tachycardia Clinical Trial
Official title:
INTERVENE: Indian Trial of Endocardial Ventricular Substrate Ablation to Prevent Recurrent VT Events
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.
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.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT03453645 -
Modification of Rhythmic Risk Assessment by Ventricular Tachycardia Ablation
|
||
Completed |
NCT05970120 -
A Study of Intracardiac Ultrasound With the NUVISION NAV Ultrasound Catheter
|
N/A | |
Completed |
NCT05791032 -
Sub Chronic Evaluation for ATP With an Extravascular Placed ICD Lead (STEP ICD) Study
|
N/A | |
Completed |
NCT04011631 -
Evaluation of the iD-SystemTM, One-Handed Disposable Internal Defibrillation System.
|
N/A | |
Recruiting |
NCT03536052 -
Ablation at Virtual-hEart pRedicted Targets for VT
|
N/A | |
Not yet recruiting |
NCT06063811 -
Ventricular Tachycardia Ablation in LVAD Patients
|
||
Enrolling by invitation |
NCT02962076 -
Study of Cardiac PET/CT Imaging to Guide Ablation Treatment of Ventricular Tachycardia
|
Early Phase 1 | |
Not yet recruiting |
NCT02784912 -
Biomarkers in Risk Stratification of Sustainted Ventricular Tachycardia or Electrical Storm After Ablation
|
N/A | |
Completed |
NCT01791543 -
Intramural Needle Ablation for Ablation of Recurrent Ventricular Tachycardia
|
N/A | |
Terminated |
NCT02891863 -
Low Energy Therapy to Convert Ventricular Tachycardias
|
Phase 0 | |
Terminated |
NCT01546207 -
Stepwise Approach To sUbstrate Modification for Ventricular Tachycardia
|
N/A | |
Completed |
NCT01294267 -
Percutaneous Hemodynamic Support With Impella 2.5 During Scar-related Ventricular Tachycardia Ablation
|
N/A | |
Terminated |
NCT00383799 -
Iv Amiodarone Versus Iv Procainamide to Treat Haemodynamically Well Tolerated Ventricular Tachycardia
|
Phase 4 | |
Completed |
NCT04884100 -
enHEART - Exploring Full Content of Optical Signals to Enhance Cardiac Arrhythmia Screening
|
N/A | |
Completed |
NCT04642963 -
Stereotactic Management of Arrhythmia - Radiosurgery in Treatment of Ventricular Tachycardia
|
N/A | |
Recruiting |
NCT05377216 -
Characterization of Cardiac Electrophysiological Effects of Autonomic Neuromodulation
|
Early Phase 1 | |
Not yet recruiting |
NCT04990089 -
VIVO European Observational Registry
|
||
Completed |
NCT04065893 -
Impact of Catheter Ablation of Ventricular Arrhythmias on Suboptimal Biventricular Pacing in Cardiac Resynchronization Therapy
|
||
Recruiting |
NCT03631303 -
Post-Extrasystolic Potentiation as a Predictor of Ventricular Arrhythmias
|
||
Recruiting |
NCT03611465 -
Creation of a Pace-mapping Atlas on Healthy and Pathological Hearts
|
N/A |