Clinical trial Recruiting at 1 site Observational Ages 18 and up

Targeted ablation to block scar channels that cause ventricular tachycardia

Official title: Segmental Substrate Isolation for the Treatment of Ventricular Tachycardia in Patients With Structural Heart Disease

Run by New York Medical College · NCT07814079 · Data updated 2026-11-12

This study tests whether targeted radiofrequency ablation of scar-channel exits can prevent ventricular tachycardia in patients with scarred hearts.

More Ischemic Cardiomyopathy trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment30 (estimated)
SponsorNew York Medical College
Academic / other
Locations1 site (Valhalla, New York)
StatusRecruiting
StartedMarch 27, 2025
Main results expectedDecember 9, 2027
Study endsDecember 9, 2028
Registry record updatedSeptember 10, 2026
Trial IDNCT07814079 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with structural heart disease undergoing VT ablation and with identifiable scar substrate.

Probably not a fit

Patients without detectable substrate during initial voltage mapping or with contraindications to ablation may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study maps channels within scar tissue that conduct impulses causing ventricular tachycardia and then delivers targeted ablation near the identified exits. It uses noninvasive mapping to guide invasive high-density substrate and activation mapping during VT ablation, followed by ablation to block the exits. After ablation, the protocol includes attempting to induce VT again to evaluate immediate success and one-year outcomes. The approach relies on pacing within the scar to identify exit sites and uses proximal ablation around mapped exits to prevent reentry. Noninvasive mapping aims to streamline the invasive procedure and focus energy delivery within a small substrate area.

Why it matters

Potential benefit: If successful, patients may have a reduced risk of VT recurrences and related hospitalizations.

How similar studies have gone: Prior studies using substrate mapping and targeted ablation for VT have shown reductions in VT episodes, though this exact exit-site–oriented approach adds novel emphasis on Scar-channel blockade.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients with structural heart disease undergoing VT ablation

Exclusion Criteria:

1. Unable or unwilling to sign consent
2. Cardiogenic shock or NYHA Class IV heart failure and not a candidate for mechanical circulatory support for the procedure (percutaneous left ventricular assist device (LVAD), extracorporeal membrane oxygenation, or implanted LVAD)
3. Absence of substrate during initial voltage mapping

Where it's running

  • Westchester Medical Center
    Valhalla, New York, United States
    Recruiting

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.