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.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | New York Medical College Academic / other |
| Locations | 1 site (Valhalla, New York) |
| Status | Recruiting |
| Started | March 27, 2025 |
| Main results expected | December 9, 2027 |
| Study ends | December 9, 2028 |
| Registry record updated | September 10, 2026 |
| Trial ID | NCT07814079 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
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.