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NCT Number: NCT06360939

Radiotherapy vs Catheter Ablation for Ventricular Tachycardia in Structural Heart Disease

The goal of this randomized clinical trial is to test the efficacy of stereotactic body radiation therapy (SBRT) in treating ventricular tachycardia (VT) in patients with advanced structural heart disease. The main questions it aims to answer are:

* What is the efficacy of SBRT compared to catheter ablation (CA) in achieving a ≥ 75% reduction in VT burden at 6 months * What is the comparable safety profile of SBRT vs CA Researchers will compare SBRT and CA (standard of care).

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Westmead Hospital

Westmead, Australia

Location status: Recruiting

Location contact

A/Prof Kumar

CONTACT

[email protected]

02 8890 8140

Saurabh Kumar

PRINCIPAL_INVESTIGATOR

About this study

Hypothesis

We hypothesise that in an open label randomised controlled trial of patients with advanced structural heart disease and ventricular tachycardia (VT) that stereotactic body radiation therapy (SBRT) will be superior in reducing VT burden compared to standard care comprising of catheter ablation (CA) and routine medical care with acceptable safety and adverse events.

Aims

This is a trial to examine if in an open label randomised trial of 60 patients with structural heart disease and VT followed for 3 years with a minimum follow up of 1 year of SBRT compared CA results in:

  • An improvement in a primary outcome of proportion of patients with a ≥75% reduction in VT burden in the 6 months following intervention compared to the 6 months intervention
  • Comparable safety profile (serious adverse events [SAE] and adverse events of special interest [AESI] at 6 months;
  • reduction in secondary endpoints at 6, 12, 24 and 36 months of: any VT recurrence, absolute % reduction in VT burden compared to 6 months pre-treatment, number of anti-arrhythmic drugs (AADs) compared to pre-treatment, cardiovascular hospitalisation, all-cause mortality, cardiac transplantation, combined endpoint of cardiovascular hospitalisation/transplant/mortality, SAE and AESI from treatment, ventricular function abd change of quality of life (QOL) metrics (at 12 months).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Structural heart disease (including ischaemic cardiomyopathy , non-ischaemic cardiomyopathy or congenital heart disease and defined as any one of
  • segmental or global decreased ventricular wall motion as defined by TTE, CT or cMRI
  • myocardial hypertrophy
  • myocardial scar (evidenced by late gadolinium enhancement on cMRI, wall thinning on cardiac CT, low voltage on electrophysiological study or abnormal intracardiac echocardiography)
  • Recurrent monomorphic VT which can include
  • at least one episode of VT treated by ICD and/or
  • sustained VT (lasting >30s) and/or
  • inducible sustained VT on invasive electrophysiological study (EPS) or non-invasive programmed stimulation (NIPS)
  • PAINESD score of ≥9 points and/or at least moderate risk of VT recurrence or death as defined by the I-VT score. Both are validated tools used clinically to identify patient at high risk of VT recurrence and/or mortality after CA.

Exclusion criteria

  • Age < 18 years
  • Life expectancy < 3 months
  • Catheter ablation deemed futile or with prohibitive risk by cardiac electrophysiologist.
  • Unwilling or unable to provide consent
  • Known cardiac channelopathies (e.g. Catecholaminergic polymorphic ventricular tachycardia (CPVT), long- or short QT syndrome, Brugada syndrome)
  • Contraindications to radiotherapy as deemed by referring physician and/or radiation oncologist
  • Pregnancy or breast feeding

Treatment and study plan

SBRT

Radiation

Delivery of 25Gy in a single dose fraction to target area within 6 weeks of randomization

CA

Procedure

CA (endocardial and/or epicardial at operator discretion) within 6 weeks of randomization.

Primary outcomes

  1. VT burden

    Time frame: 6 months

    Change in proportion of patients with a ≥75% reduction in VT burden at 6 months (number of VT episodes in 6 months post treatment compared to the number of VT episodes in the 6 months prior to randomisation excluding a 6-week blanking period after treatment initiation)

Secondary outcomes

  1. Recurrent sustained VT

    Time frame: 6, 12, 24 and 36 months

    Recurrent sustained VT ascertained by implanted cardioverter defibrillator (ICD) (VT identified and treated by the ICD with anti-tachycardia pacing (ATP) and/or internal ICD delivered shock or ≥30 seconds of VT if untreated by ICD

  2. VT storm

    Time frame: 6, 12, 24 and 36 months

    VT storm (three or more documented episodes of VT within 24 hours or incessant VT)

  3. Absolute VT burden

    Time frame: 6, 12, 24 and 36 months

    Absolute percentage reduction in VT burden compared to pre-ablation

  4. Serious Adverse Events (SAE) and Adverse Events of Special Interest (AESI)

    Time frame: At all time points up to 36 months

    • SAE and AESI related to effects of SBRT
    • SAE and AESI related to standard care e.g. medical anti-arrhythmic drug therapy or catheter ablation or heart transplantation
  5. ICD shocks

    Time frame: 6, 12, 24 and 36 months

    Implantable Cardioverter Defibrillator shocks

  6. Hospitalization

    Time frame: 6, 12, 24 and 36 months

    Cardiovascular as well as specifically heart failure and arrhythmia

  7. All cause mortality

    Time frame: 6,12, 24 and 36 months

    All cause mortality

  8. Cardiovascular Mortality

    Time frame: 6,12, 24 and 36 months

    Cardiovascular mortality

  9. Composite outcome of VT recurrence/hospitalisation/death/ cardiac transplantation

    Time frame: 6,12, 24 and 36 months

    Composite outcome as above

  10. Ventricular function

    Time frame: 6,12, 24 and 36 months

    As determined by echocardiography (ejection fraction, speckle tracking echocardiography)

  11. Quality of Life as per Short Form - 36 (SF-36) Score

    Time frame: 6,12, 24 and 36 months

    Change in quality of life at 6 and 12 months (compared to pre-intervention) as measured by Short Form- 36 (SF-36) [0-100 scale, 0 is equivalent to maximum disability and a score of 100 is equivalent to no disability].

  12. Quality of Life as per Implantable Cardioverter Defibrillator Concerns Questionnaire (ICDC) score

    Time frame: 6,12, 24 and 36 months

    Change in quality of life at 6 and 12 months (compared to pre-intervention) as measured by Implantable Cardioverter Defibrillator Concerns Questionnaire (ICDC) score. [0-100 scale, 100 equivalent to maximum concern]

  13. Number of AADs

    Time frame: 6,12, 24 and 36 months

    Number of AADs at time points following randomization

Study contacts

Contact information is provided by the study sponsor or research team.

Saurabh Kumar, MBBS | PhD

CONTACT

[email protected]

(02)88908140 ext. +61

Sponsors and collaborators

Lead sponsor

Western Sydney Local Health District

Other

Collaborators

  • National Heart Foundation, Australia
  • University of Sydney

Registry information

Acronym: RadioAblate-VT

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Apr 11, 2024
Registry last updated
Feb 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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