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NCT05225935Completed

Computed Tomography-Guided Catheter Ablation for Ventricular Tachycardia

Computed Tomography-Guided Catheter Ablation for Ventricular Tachycardia (InEurHeart Study)

Source: ClinicalTrials.gov · Last updated 22 May 2026

Brief summary (registry, in English)

This double arm randomized study will compare 2 ventricular tachycardia ablation strategies: the standard strategy based on invasive substrate and VT mapping with 3D electro-anatomical system vs a tailored strategy which identifies targets based on pre-procedural CT-scan imaging. The primary endpoint will be procedure duration and secondary endpoints will include safety and efficacy criteria as well as medico-economic evaluation.

Status (registry)
Completed
Study type
Interventional
Enrollment
119 (actual)
First submitted
25 Jan 2022
Start date
29 Jun 2022
Primary completion date
22 Dec 2023
Lead sponsor
University Hospital, Bordeaux
NCT number
NCT05225935

What you commit to

  • Study type: Interventional
  • Participants enrolled: 119
  • From 29 Jun 2022 to the primary completion date, 22 Dec 2023
  • 14 sites in 4 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Have had a prior catheter ablation procedure for VT,

Other illness

  • Active ischemia (acute thrombus diagnosed by coronary angiography, or dynamic ST segment changes demonstrated on ECG) or another reversible cause of VT (e.g. drug-induced arrhythmia), had recent acute coronary syndrome within 30 days thought to be due to acute coronary arterial thrombosis, or have CCS functional class IV angina. Note that biomarker level elevation alone after ventricular arrhythmias does not denote acute coronary syndrome or active ischemia,
  • Presenting arrhythmia: polymorphic VT or ventricular fibrillation (VF),

Lab values

  • Renal failure (Creatinine clearance \<30 mL/min), have NYHA Functional class IV heart failure, or a systemic illness likely to limit survival to \<1 year,

Other

  • Unable to understand the nature, risks, significance and implications of the clinical investigation or unwilling to provide written informed consent,
  • Are known to have protruding left ventricular thrombus or mechanical aortic and mitral valves,
  • Women who are pregnant, lactating, or who are planning to become pregnant during the anticipated study period,
  • Patient under legal protection

Who the study is looking for

  • Age ≥ 18 years,
  • Indication for catheter ablation intervention with planned preoperative cardiac CT scan
  • Prior myocardial infarction (using the international definition of MI: Q waves or imaging evidence of regional myocardial akinesis/thinning in the absence of a non- ischemic cause with documentation of prior ischemic injury),
  • Presence of an implantable cardioverter defibrillator, or planned ID implantation before discharge, and
  • One of the following monomorphic VT events within last 6 months:
    • A: ≥3 episodes of VT treated with antitachycardia pacing (ATP),
    • B: ≥1 appropriate ICD shocks,
    • C: sustained VT below detection rate of the ICD documented by ECG or any cardiac monitor
    • D: Sustained VT recorded on 12 leads ECG in the absence of ICD
  • Highly effective contraception for women of childbearing potential, maintained during research procedures
  • Signed informed consent ,
  • Affiliated to or beneficiary of a health insurance

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (14)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Medical University of Graz
Coordinator of this site? Confirm its status
GrazAustriaUnknown status
Public Hospital Elisabethinen Linz
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LinzAustriaUnknown status
Inselspital Universitätsspital Bern
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BernSwitzerlandUnknown status
Vaudois University Hospital, Lausanne
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LausanneSwitzerlandUnknown status
Rhön-Klinikum AG
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Bad Neustadt an der SaaleGermanyUnknown status
Evangelisches Krankenhaus Düsseldorf
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DüsseldorfGermanyUnknown status
Asklepios Klinik St. Georg Hamburg
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HamburgGermanyUnknown status
Universitätsklinikum Schleswig-Holstein
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LübeckGermanyUnknown status
Deutsches Herzzentrum München
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MünchenGermanyUnknown status
CHU de Clermont-Ferrand
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Clermont-FerrandFranceUnknown status
CHU de Limoges
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LimogesFranceUnknown status
APHP Salpétrière
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ParisFranceUnknown status
CHU de Bordeaux
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PessacFranceUnknown status
CHU de Toulouse
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ToulouseFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.