Actively Recruiting

Phase 2
Age: 18Years +
All Genders
NCT05439031

StereoTactic Arrhythmia Radiotherapy in the NetherLands no. 2

Led by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Updated on 2026-01-14

12

Participants Needed

1

Research Sites

214 weeks

Total Duration

On this page

Sponsors

A

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Lead Sponsor

D

Dutch Heart Foundation

Collaborating Sponsor

AI-Summary

What this Trial Is About

Ventricular tachycardia (VT) is a malignant cardiac arrhythmia subjecting our patients to a high risk of sudden death, increased morbidity and reduced quality of life. Unfortunately, failure of treatment is common and VT recurrences remain an important concern. In these patients, stereotactic arrhythmia radiotherapy appears to be an effective and safe treatment. The mechanism of action however remains unknown and should be elucidated. The objective of this phase 2, single arm, monocenter, pre-post intervention study is to evaluate the efficacy and safety of stereotactic arrhythmia radiotherapy and obtain insights in the mechanism of action by evaluating electro-anatomical alterations of stereotactic arrhythmia radiotherapy in patients with therapy refractory ventricular tachycardia.

CONDITIONS

Official Title

StereoTactic Arrhythmia Radiotherapy in the NetherLands no. 2

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Implanted implantable cardioverter defibrillator (ICD)
  • WHO/ECOG performance status grade 0-3 in the past 3 months
  • At least 3 episodes of treated ventricular tachycardia within the last 3 months
  • Recurrence of ventricular tachycardia after failed or intolerant to at least one class 1 or class 3 anti-arrhythmic drug AND at least one catheter ablation procedure OR considered unsuitable for catheter ablation
  • Able and willing to undergo all necessary evaluations, treatment, and follow-up for the study and afterward
Not Eligible

You will not qualify if you...

  • Pregnancy
  • History of radiation treatment in the thorax or upper abdominal region
  • Interstitial pulmonary disease

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
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Trial Site Locations

Total: 1 location

1

Amsterdam UMC location University of Amsterdam

Amsterdam, North Holland, Netherlands, 1105AZ

Actively Recruiting

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Research Team

P

Pieter G Postema, MD PhD

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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