Endo-epicardial vs Endocardial-only Catheter Ablation of Ventricular Tachycardia in Patients With Ischemic Cardiomyopathy (EPIC-VT)
Launched by RENNES UNIVERSITY HOSPITAL · May 24, 2023
Trial Information
Current as of July 22, 2025
Recruiting
Keywords
ClinConnect Summary
The EPIC-VT clinical trial is researching the best way to treat a heart condition called ventricular tachycardia (VT) in patients with ischemic cardiomyopathy, which is heart disease caused by reduced blood flow to the heart. The study aims to compare two methods of a procedure called catheter ablation, which helps to stop the irregular heartbeats. One method uses only an endocardial approach, which means that the treatment is done from inside the heart. The other method combines both endocardial and epicardial approaches, which treats the heart from both inside and outside. Researchers want to find out if the combined approach can lower the chances of VT coming back compared to the endocardial-only approach.
To participate in this trial, individuals must be at least 18 years old and are having their first catheter ablation for VT related to ischemic heart disease. They should also have an implantable cardioverter-defibrillator (ICD) and be able to provide informed consent. Participants can expect to undergo either of the two treatment methods, and the study is currently recruiting patients. It’s important to note that certain medical histories or current treatments may prevent someone from joining, such as previous heart surgeries or certain medications. This trial is crucial because reducing the recurrence of VT can significantly improve heart health and overall well-being in patients with this condition.
Gender
ALL
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
About Rennes University Hospital
Rennes University Hospital, a leading academic medical center in France, is dedicated to advancing healthcare through innovative clinical research and trials. With a strong emphasis on patient-centered care, the hospital integrates cutting-edge scientific research with clinical practice, fostering collaboration among multidisciplinary teams. Its commitment to excellence is reflected in its robust infrastructure and expertise in various medical fields, enabling the development and evaluation of novel therapies and treatment protocols. By participating in clinical trials, Rennes University Hospital aims to enhance patient outcomes and contribute to the global body of medical knowledge.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Paris, , France
Nantes, , France
Lille, , France
Rennes, , France
Lyon, , France
Bordeaux, , France
Caen, , France
Saint étienne, , France
Clermont Ferrand, , France
Paris, , France
Toulouse, , France
Tours, , France
Patients applied
Trial Officials
Raphaël MARTINS, MD, PhD
Principal Investigator
Rennes University Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported