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Preventive VT Substrate Ablation in Ischemic Heart Disease (PREVENT-VT)

Primary Purpose

Ventricular Tachycardia, Ventricular Arrythmia, Sudden Cardiac Death

Status
Recruiting
Phase
Phase 3
Locations
Spain
Study Type
Interventional
Intervention
Ventricular tachycardia substrate-based radiofrequency ablation
Sponsored by
Centro Medico Teknon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ventricular Tachycardia focused on measuring ventricular tachycardia, ventricular arrhythmia, sudden cardiac death, ischemic heart disease, cardiac magnetic resonance, border zone channels

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age > 18 years.
  • Chronic, stable ischemic heart disease, irrespectively of the LVEF.
  • Life expectancy of > 1 year with a good functional status.
  • Documented scar AND a BZC mass > 5.15 g as measured per LGE-CMR and automatic post-processing using the ADAS-3D LV (ADAS 3D Medical SL, Barcelona, Spain).
  • Signed informed consent.

Exclusion Criteria:

  • Age < 18 years.
  • Pregnancy.
  • Life expectancy of < 1 year, or bad functional status (NYHA IV functional class).
  • Other concomitant structural heart diseases (e.g. congenital, non-ischemic, etc.)
  • Previously documented sustained ventricular arrhythmias.
  • Impossibility to perform a contrast-enhanced CMR study.
  • Calculated BZC mass in the scarred tissue < 5.15 g using the ADAS-3D LV software.
  • Concomitant investigation treatments.
  • Medical, geographical and social factors that make study participation impractical, and inability to give written informed consent. Patient's refusal to participate in the study.

Sites / Locations

  • Centro Medico TeknonRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

ABLATE arm

NO-TREAT arm

Arm Description

Ventricular tachycardia substrate ablation intending to: i) eliminate all the potential arrhythmogenic substrate, aiming for complete electrical isolation/elimination of all the electrograms with delayed components or showing hidden slow conduction properties, and ii) non-inducibility or ventricular tachycardias at the end of the procedure. Standard medical treatment will also be given for these patients.

Only standard medical treatment will be offered for these patients.

Outcomes

Primary Outcome Measures

Rate of sudden cardiac death or sustained ventricular tachycardia
Composite outcome of sudden cardiac death or sustained ventricular tachycardia (either treated by an ICD or documented with continuous Holter monitoring) in patients undergoing preventive ventricular tachycardia (VT) substrate ablation vs. standard of care.

Secondary Outcome Measures

Procedure time
Procedure time
Radiofrequency time
Radiofrequency time
Rate of achievement of complete substrate ablation
Rate of achievement of complete substrate ablation
VT inducibility rate
Final VT inducibility rate
Rate of complications
Rate of complications
Rate of need for anti-arrhythmic drugs
Rate of need for anti-arrhythmic drugs in both arms of the study

Full Information

First Posted
November 29, 2020
Last Updated
August 29, 2023
Sponsor
Centro Medico Teknon
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1. Study Identification

Unique Protocol Identification Number
NCT04675073
Brief Title
Preventive VT Substrate Ablation in Ischemic Heart Disease
Acronym
PREVENT-VT
Official Title
Preventive VT Substrate Ablation in Patients With Chronic Post-MI Scar Showing Arrhythmogenic Characteristics
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 1, 2021 (Actual)
Primary Completion Date
June 2025 (Anticipated)
Study Completion Date
December 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centro Medico Teknon

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The investigators hypothesize that preventive VT substrate ablation in patients with chronic ICM, previously selected based on imaging criteria (BZC mass) for their likely high arrhythmic risk, is safe and effective in preventing clinical VT events.
Detailed Description
Fibrotic tissue is known to be the substrate for the appearance of scar-related reentrant ventricular arrhythmias (VA) in chronic ischemic cardiomyopathy (ICM). Late gadolinium enhancement cardiac magnetic resonance (LGE-CMR) has proven to be a useful technique in the non-invasive characterization of the scarred tissue and the underlying arrhythmogenic substrate. Previous studies identified the presence of significant scarring (>5% of the LV mass) is an independent predictor of adverse outcome (all-cause mortality or appropriate ICD discharge for ventricular tachycardia or fibrillation) in patients being considered for implantable cardioverter-defibrillator (ICD) placement. Parallelly, the presence of heterogeneous tissue channels, which correlate with voltage channels after endocardial voltage mapping of the scar, can be more frequently observed in patients suffering from SMVT than in matched controls for age, sex, infarct location, and LVEF. However, the lack of solid evidence and randomized trials make LVEF still the main decision parameter when assessing suitability for ICD implantation in primary prevention of SCD. (7,8) In a recent, case-control study, the investigators identified the BZC mass as the only independent predictor for VT occurrence, after matching for age, sex, LVEF and total scar mass. This BZC mass can be automatically calculated using a commercially available, post-processing imaging platform named ADAS 3D LV (ADAS3D Medical SL, Barcelona, Spain), with FDA 510(k) Clearance and CE Mark approval. Thus, CMR-derived BZC mass might be used as an automatically reproducible criterium to reclassify those patients with chronic ICM at highest risk for developing VA/SCD in a relatively short period of time (approx. 2 years). On the other hand, catheter ablation has become an essential tool in the treatment of ventricular arrhythmias in patients with structural heart disease (SHD). VT ablation techniques have evolved towards substrate-based approaches that permit to abolish multiple VT circuits irrespective of their inducibility or hemodynamic tolerability, improving outcomes with respect to clinical VT ablation. Moreover, VT substrate ablation procedures performed during sinus rhythm and CMR-guided have proven to be safe, with very low procedure related complications. The investigators hypothesize that preventive VT substrate ablation in patients with chronic ICM, previously selected based on imaging criteria (BZC mass) for their likely high arrhythmic risk, is safe and effective in preventing clinical VT events.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ventricular Tachycardia, Ventricular Arrythmia, Sudden Cardiac Death, Sudden Cardiac Death Due to Cardiac Arrhythmia, Ischemic Heart Disease, Myocardial Infarction, Magnetic Resonance Imaging
Keywords
ventricular tachycardia, ventricular arrhythmia, sudden cardiac death, ischemic heart disease, cardiac magnetic resonance, border zone channels

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
58 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ABLATE arm
Arm Type
Experimental
Arm Description
Ventricular tachycardia substrate ablation intending to: i) eliminate all the potential arrhythmogenic substrate, aiming for complete electrical isolation/elimination of all the electrograms with delayed components or showing hidden slow conduction properties, and ii) non-inducibility or ventricular tachycardias at the end of the procedure. Standard medical treatment will also be given for these patients.
Arm Title
NO-TREAT arm
Arm Type
No Intervention
Arm Description
Only standard medical treatment will be offered for these patients.
Intervention Type
Procedure
Intervention Name(s)
Ventricular tachycardia substrate-based radiofrequency ablation
Intervention Description
The CARTO3 electroanatomic navigation system (Biosense Webster, Diamond Bar, CA, USA) will be used for ablation. An open irrigated 3.5-mm tip ablation catheter (ThermoCool SmartTouch, Biosense Webster, Diamond Bar, CA, USA) will be used for mapping and ablation. The first step of the procedure will be the acquisition of a fast-anatomical map (FAM) of the aorta. This FAM will be then used to integrate the multi-detector cardiac tomography (MDCT) reconstruction and cardiac magnetic resonance (CMR)-derived pixel-signal intensity (PSI) maps within the spatial reference coordinates of the CARTO3 system. RF will be delivered at the entrance of the border zone channels (BZCs) identified in the PSI maps (CMR-guided scar dechanneling technique). Programmed ventricular stimulation (PVS) will be always performed after substrate elimination to test for final inducibility.
Primary Outcome Measure Information:
Title
Rate of sudden cardiac death or sustained ventricular tachycardia
Description
Composite outcome of sudden cardiac death or sustained ventricular tachycardia (either treated by an ICD or documented with continuous Holter monitoring) in patients undergoing preventive ventricular tachycardia (VT) substrate ablation vs. standard of care.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Procedure time
Description
Procedure time
Time Frame
2 years
Title
Radiofrequency time
Description
Radiofrequency time
Time Frame
2 years
Title
Rate of achievement of complete substrate ablation
Description
Rate of achievement of complete substrate ablation
Time Frame
2 years
Title
VT inducibility rate
Description
Final VT inducibility rate
Time Frame
2 years
Title
Rate of complications
Description
Rate of complications
Time Frame
2 years
Title
Rate of need for anti-arrhythmic drugs
Description
Rate of need for anti-arrhythmic drugs in both arms of the study
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 years. Chronic, stable ischemic heart disease, irrespectively of the LVEF. Life expectancy of > 1 year with a good functional status. Documented scar AND a BZC mass > 5.15 g as measured per LGE-CMR and automatic post-processing using the ADAS-3D LV (ADAS 3D Medical SL, Barcelona, Spain). Signed informed consent. Exclusion Criteria: Age < 18 years. Pregnancy. Life expectancy of < 1 year, or bad functional status (NYHA IV functional class). Other concomitant structural heart diseases (e.g. congenital, non-ischemic, etc.) Previously documented sustained ventricular arrhythmias. Impossibility to perform a contrast-enhanced CMR study. Calculated BZC mass in the scarred tissue < 5.15 g using the ADAS-3D LV software. Concomitant investigation treatments. Medical, geographical and social factors that make study participation impractical, and inability to give written informed consent. Patient's refusal to participate in the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Antonio Berruezo, MD, PhD
Phone
(+34) 93 290 62 51
Email
antonio.berruezo@quironsalud.es
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Antonio Berruezo, MD, PhD
Organizational Affiliation
Centro MΓ©dico Teknon
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centro Medico Teknon
City
Barcelona
ZIP/Postal Code
08022
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Antonio Berruezo, MD, PhD
Phone
+34932906200
Email
antonio.berruezo@quironsalud.es
First Name & Middle Initial & Last Name & Degree
Antonio Berruezo, MD, PhD
First Name & Middle Initial & Last Name & Degree
Diego Penela, MD, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
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Preventive VT Substrate Ablation in Ischemic Heart Disease

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