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Recruiting NCT05888662

NCT05888662 Endo-epicardial vs Endocardial-only Catheter Ablation of Ventricular Tachycardia in Patients With Ischemic Cardiomyopathy (EPIC-VT)

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Clinical Trial Summary
NCT ID NCT05888662
Status Recruiting
Phase
Sponsor Rennes University Hospital
Condition Ischemic Cardiomyopathy
Study Type INTERVENTIONAL
Enrollment 150 participants
Start Date 2023-10-23
Primary Completion 2029-10-23

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Endo-epicardial ablationendocardial ablation only

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 150 participants in total. It began in 2023-10-23 with a primary completion date of 2029-10-23.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Radiofrequency ablation of ventricular tachycardias (VTs) is the gold standard treatment of refractory VTs in patients with ischaemic heart disease. In this setting, ablation is usually performed endocardially. However, even after a procedural success there is a high risk of recurrence, particularly due to the inability to create transmural lesions. Indeed, only the endocardium of the LV has been ablated, while a significant part of the arrhythmia substrate may be located on the other side of the myocardial thickness, on the epicardial side of the LV. First described in 1996, epicardial ablation, performed via a percutaneous subxyphoid approach, has since undergone considerable development. Electrophysiologists often use a double endo- and epicardial approach as first line therapy for the ablation of VTs complicating myocarditis or arrhythmogenic dysplasia of the right ventricle, where the substrate is most often epicardial. For VT in ischaemic heart disease, electrophysiologists perform endocardial ablation, and often perform epicardial ablation only after several endocardial failures. Several observational studies suggest that a combined endo- and epicardial approach as first line therapy is associated with a reduced risk of VT recurrence. Since recurrent VT in patients with ischaemic heart disease as a prognostic impact in terms of morbidity and mortality, it appears essential to optimise rhythm management by ablation, by offering a combined approach from the as first approach to reduce the risk of recurrences. The aim of our prospective, multicentre, controlled, randomized study is therefore to compare the rate of VT recurrence after ablation performed as first line therapy either by endocardial approach alone or by combined endo-epicardial approach.

Eligibility Criteria

Inclusion Criteria: 1. Patients over 18 years of age 2. 1st radiofrequency ablation of VT complicating ischaemic heart disease 3. Patients with an ICD and remote monitoring 4. Having, for women of childbearing age, effective contraception until discharge from hospital 5. Have given their free and informed consent in writing 6. are affiliated to or have health insurance Exclusion Criteria: 1. History of cardiac surgery compromising the epicardial approach (coronary artery bypass grafting, valve replacements, or other surgeries that may have caused pericardial adhesions) 2. Presence of a left intraventricular thrombus found during pre-procedure imaging 3. Anticoagulant therapy that cannot be temporarily discontinued 4. Double antiplatelet therapy that cannot be temporarily replaced by single antiplatelet therapy 5. History of pericarditis 6. Previous thoracic radiotherapy 7. Contraindication to general anaesthesia 8. Pregnant or breastfeeding woman 9. History of heparin-induced thrombocytopenia type 2 (as injection is required during the procedure) 10. Person under legal protection (safeguard of justice, curatorship, guardianship), deprived of liberty, or unable to express consent

Contact & Investigator

Central Contact

Raphaël MARTINS, MD, PhD

✉ raphael.martins@chu-rennes.fr

📞 299282517

Principal Investigator

Raphaël MARTINS, MD, PhD

PRINCIPAL INVESTIGATOR

Rennes University Hospital

Frequently Asked Questions

Who can join the NCT05888662 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Ischemic Cardiomyopathy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05888662 currently recruiting?

Yes, NCT05888662 is actively recruiting participants. Contact the research team at raphael.martins@chu-rennes.fr for enrollment information.

Where is the NCT05888662 trial being conducted?

This trial is being conducted at Bordeaux, France, Caen, France, Clermont-Ferrand, France, Lille, France and 8 additional locations.

Who is sponsoring the NCT05888662 clinical trial?

NCT05888662 is sponsored by Rennes University Hospital. The principal investigator is Raphaël MARTINS, MD, PhD at Rennes University Hospital. The trial plans to enroll 150 participants.

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