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
- Diseases
- Coronary artery disease
- 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
Sites (14)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Medical University of Graz Coordinator of this site? Confirm its status | Graz | Austria | Unknown status |
| Public Hospital Elisabethinen Linz Coordinator of this site? Confirm its status | Linz | Austria | Unknown status |
| Inselspital Universitätsspital Bern Coordinator of this site? Confirm its status | Bern | Switzerland | Unknown status |
| Vaudois University Hospital, Lausanne Coordinator of this site? Confirm its status | Lausanne | Switzerland | Unknown status |
| Rhön-Klinikum AG Coordinator of this site? Confirm its status | Bad Neustadt an der Saale | Germany | Unknown status |
| Evangelisches Krankenhaus Düsseldorf Coordinator of this site? Confirm its status | Düsseldorf | Germany | Unknown status |
| Asklepios Klinik St. Georg Hamburg Coordinator of this site? Confirm its status | Hamburg | Germany | Unknown status |
| Universitätsklinikum Schleswig-Holstein Coordinator of this site? Confirm its status | Lübeck | Germany | Unknown status |
| Deutsches Herzzentrum München Coordinator of this site? Confirm its status | München | Germany | Unknown status |
| CHU de Clermont-Ferrand Coordinator of this site? Confirm its status | Clermont-Ferrand | France | Unknown status |
| CHU de Limoges Coordinator of this site? Confirm its status | Limoges | France | Unknown status |
| APHP Salpétrière Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| CHU de Bordeaux Coordinator of this site? Confirm its status | Pessac | France | Unknown status |
| CHU de Toulouse Coordinator of this site? Confirm its status | Toulouse | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.