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OpenTrials
Completed

NCT Number: NCT07590908

CARA-VT: a Dosimetric in Silico Study

Ventricular tachycardia (VT) is a potentially deadly condition, common in patients with structural heart disease or dilated cardiomyopathy. VTpatients are currently treated with anti-arrhythmic drugs, implanted cardioverter defibrillators or invasive catheter ablation (CA) but the overall success rate of this techniqueis still suboptimal.

One of the main reasons is an anatomically inaccessible location of VT's origin (within the mid-wall of the myocardium, on the epicardial site or adjacent to critical structures). Moreover, repeated invasive ablation, technical difficulties or patient comorbidities can lead to non-eligibility for CA. Accordingly, a rationale exists to adopt more effective and less invasive therapies.

A promising novel non-invasive treatment option for refractory VT is stereotactic arrhythmia radio-ablation (STAR), originally born for cancer treatment, which consists in the application of high-energy photons in a single 25 Gy dose to limited areas of the ventricles, also to those inaccessible for CA, recognized through non-invasive surface ECG-mapping as the origin of VT. Preliminary small case series described good tolerance and improved VT burden during follow-up.

Due to the encouraging physical and biological characteristics of protons and carbon ions, the dose to surrounding healthy tissues could potentially be better spared in comparison with photons. Especially, the cardiac healthy sub-structures might benefit from the use of particle beams instead of photons. On the other hand, due to range uncertainties affecting particle beams, delivering an ideal radiation treatment with heavy ions to fast-moving targets such as the heart, is more complex. So far, the feasibility and the safety of cardiac radiotherapy with protons and heavy ions have only been evaluated in animal models and recently in the first in man case managed by the collaboration between CNAO and San Matteo Cardiology Department in a patient treated with compassionate aim.

To date, feasibility and safety data showing potential advantages of particles over photon therapy in dose distributions are missing.

Therefore, we propose a study aimed to compare different radiation therapy treatment modalities (photons vs. particle therapy: protons and carbon ions) simulating the RT treatment of ventricular arrhythmias on real patients candidates to invasive catheter ablation treatment.

STAR with photons was first reported in 2013 and an increasingly number of case reports and case series have been published ever since, showing an acceptable safety profile and promising efficacy.

Decreasing the dose to the surrounding healthy heart tissues is expected to be very advantageous for patients.

Particle therapy based on its dosimetric physical selectivity compared to SBRT (Stereotactic Body Radiotherapy) with photons might have the potential to both lower off-target doses and lower risk of possible side effects.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

SC Cardiologia, Fondazione IRCCS Policlinico San Matteo

Pavia, 27100, Italy

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Recurrent VT with clinical indication to receive catheter ablation
  • Written informed consent
  • Patient's ability to understand the characteristics and consequences of the clinical study
  • Invasive mapping data

Exclusion criteria

  • Allergy to iodinated contrast media
  • Pregnancy and breastfeeding
  • Younger than 18 years

Treatment and study plan

Primary outcomes

  1. Feasibility of particle therapy (protons and carbon ions)

    Time frame: up to 3 years

    To verify the feasibility of particle therapy plans in patients with refractory VT.

    Plans will be considered feasible whether the dosimetric criteria outlined will be achieved in no fewer than 90% of enrolled patients (30 enrolled patients).

  2. Dose sparing on surrounding non-target tissues with particle therapy (protons and carbon ions)

    Time frame: up to 3 years

    To compare simulated RT plans with protons, carbon ions and photons, and quantify the differences in terms of dose released to surrounding cardiac and non-cardiac healthy tissues.

    Comparison of simulated RT plans, with protons, carbon ions and photons, by using cardiac motion management, optimizing the treatment plan on different cardiac phases at ECG-gated CT scan and ECG-gated radiotherapy beams delivery, for the same cardiac targets, will be done in terms of planned target coverage (target conformity index) and dose-volume histograms (DVH).

Secondary outcomes

  1. Integration of ECGi Mapping into Planning CT for Target Contouring

    Time frame: up to 3 years

    To collect preliminary data of non-invasive electrocardiographic mapping (ECGi) usage for target definition in the setting of STAR, including the possibility of directly incorporating ECGi non-invasive mapping data into the planning CT to minimize potential mistakes in contouring the target.

  2. Feasibility and interferences of Ultrasound Probe on RT treatment planning

    Time frame: up to 3 years

    To verify the feasibility and possible interferences with simulated RT treatment planning of the use of an ultrasound probe (for online cardiac localization during beam delivery), positioned on the chest wall of patients during the imaging phase.

    The feasibility will not be achieved in case the limited beam angles due to the probe position do not allow to achieve the dosimetric plan criteria outlined in table 1 in more than 10% of the enrolled patients.

  3. Development of Automatic Image Alignment

    Time frame: up to 3 years

    To develop and assess techniques for the automatic alignment of different images including CT and electroanatomic maps (EAM), to compose a single multimodal ventricular image where ablation planning can be more easily performed.

  4. Optimizing Arrhythmogenic Site Detection with Advanced Signal Processing Tools

    Time frame: up to 3 years

    To develop and assess techniques for the advanced simulation of the patient's ventricle by electrophysiological modelling customized on the EAM and the associated electrical information, to allow an in-silico test of the planned ablation strategy on a digital twin.

    Optimal identification of arrhythmogenic sites will also be pursued by the adoption of novel signal and information processing tools that have already demonstrated to be effective in the local identification of abnormal ventricular potentials.

Sponsors and collaborators

Lead sponsor

Fondazione IRCCS Policlinico San Matteo di Pavia

Other

Collaborators

  • CNAO National Center of Oncological Hadrontherapy, Pavia, Italy

Registry information

Official study title

Non-invasive CArdiac RAdioablation for Ventricular Tachycardia: a Feasibility Dosimetric in Silico Study Based on a Prospective Cohort of Patients to Compare Photon to Proton and to Carbon Ion Radiotherapy

Acronym: CARA-VT

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
May 15, 2026
Registry last updated
May 15, 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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