Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06937983

Optimised Decrement Evoked Potential (DeEP) Mapping to Guide Ventricular Tachycardia (VT) Ablation in Patients With Structural Heart Disease VT

Led by University Hospitals Coventry and Warwickshire NHS Trust · Updated on 2026-04-13

77

Participants Needed

1

Research Sites

138 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Ventricular tachycardia (VT) is a life-threatening heart rhythm disorder. Special pacemakers called implantable cardiac defibrillators (ICDs) help treat VT episodes, however they do not prevent the VT episodes from occurring. Catheter ablation for VT is a minimally-invasive and established procedure for preventing VT recurrence. This involves placing wires in the heart to find the diseased areas that are responsible for the VT episodes. The diseased areas are shown on computer-generated maps and are later removed via controlled tissue heating (ablation). A major challenge during the VT ablation procedure is locating the diseased area responsible for the VT episodes. Several methods have been described to locate the diseased heart area, however these methods are not always effective. In this study, we aim to improve the identification of the diseased heart areas responsible for the VT episodes using a novel method. Our research group have developed, tested and peer-reviewed this improved method of locating diseased areas by looking for signals called decrementing evoked potentials (DeEPs). Ablation will target DeEPs shown on the computer-generated maps. We will assess if VT can be triggered at the end of the procedure. Patients will be monitored over 12 months to see if ablation of DeEPs leads to a reduction in VT episodes. We aim to recruit 77 patients with established heart disease of any cause, who have suffered VT episodes with ICDs. Suitable patients will be identified and recruited from inpatient and outpatient settings. A quality-of-life questionnaire will be completed by patients before and after the ablation procedure. The procedure will be performed as routine standard of care, in the cardiac catheter laboratory across multiple recruiting cardiac centres in the UK providing well established VT ablation service. Overall, this study will contribute towards developing refined VT ablation techniques, aiming to improve patient outcomes.

CONDITIONS

Official Title

Optimised Decrement Evoked Potential (DeEP) Mapping to Guide Ventricular Tachycardia (VT) Ablation in Patients With Structural Heart Disease VT

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years old or older
  • Patients with cardiac implantable electronic devices such as pacemakers, cardiac resynchronisation therapy devices, or implantable cardioverter defibrillators
  • Eligible for ventricular tachycardia ablation as part of standard care, either urgent or elective
  • Diagnosed with ischaemic heart disease and prior myocardial infarction or other structural heart diseases such as arrhythmogenic cardiomyopathy, dilated cardiomyopathy, hypertrophic cardiomyopathy, sarcoidosis, or myocarditis
  • Planned catheter ablation of ventricular tachycardia using Abbott intracardiac mapping catheter and Ensite intracardiac mapping system
Not Eligible

You will not qualify if you...

  • Lacks capacity to provide informed consent
  • New York Heart Association class IV heart failure
  • Life expectancy less than 12 months
  • Implanted with a ventricular assist device
  • Presence of mobile intracardiac thrombus
  • Reversible cause of ventricular tachycardia
  • Women who are pregnant or nursing
  • Presence of both mechanical aortic and mitral valves
  • Enrolment in another interventional clinical study judged to increase risk or interfere with participation

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

University Hospitals Coventry & Warwickshire NHS Trust

Coventry, West Midlands, United Kingdom, CV2 2DX

Actively Recruiting

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Research Team

S

Shivam Joshi

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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