MRI-guided Ventricular Tachycardia Ablation in Patients With Structural Heart Disease
Key facts
- Who runs it
- China National Center for Cardiovascular Diseases
- Where
- China1 site in 1 countryChoose a country to see its sites
- Trial code
- Status
- Not yet recruiting
- People taking part
- 526 people, planned
- Started
- 1 Oct 2026
- Expected to end
- 1 Aug 2029
- Type of study
- Interventional, 2 groupsOne group gets an existing treatment, for comparison.
- Treatments tested
- LGE-MRI-integrated EAM-guided catheter ablation
- Conventional EAM-guided catheter ablation
- Record updated
- 27 October 2026
Who can take part
- Age
- 18 years to 75 years
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
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Who can take part
- Aged 18 to 75 years
- Diagnosis as SHD (including ICM and NICM)
- Documented sustained VT
Who cannot take part
- Prior ablation therapy for premature ventricular contractions or VT
- Contraindications to catheter ablation (e.g., intracardiac thrombus, decompensated heart failure)
- History of cardiac surgery
- Stroke or transient ischemic attack (TIA) within the past 6 months
- Contraindications to MRI (e.g., incompatible metallic implants, claustrophobia, or other MRI-unsafe conditions)
Check if you might fit
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 75 years old?
This trial has no sites in United States.
It has sites in one country. Choose a country to see its sites.
About the trial
What the trial wants to find out
Ventricular tachycardia (VT) is a life-threatening heart rhythm disorder that frequently occurs in patients with structural heart disease, such as ischemic or non-ischemic cardiomyopathy. In these patients, VT usually arises from re-entrant circuits within or around scar tissue in the heart muscle. Catheter ablation, which uses radiofrequency energy to eliminate the abnormal tissue responsible for VT, is an established treatment. However, its long-term success rate remains modest (about 40-60%), partly because conventional three-dimensional electroanatomical mapping (EAM) relies on voltage measurements that cannot fully reveal the complex three-dimensional scar architecture that drives the arrhythmia.
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Cardiac magnetic resonance imaging (MRI) with late gadolinium enhancement (LGE) can visualize myocardial scar in high detail before the procedure. Dedicated software (ADAS-3D) converts these MRI scans into a patient-specific three-dimensional model of the scar, including the "heterogeneous tissue channels" of surviving muscle within the scar that are the likely source of VT. This model can be integrated into the mapping system during the ablation procedure, potentially allowing operators to identify and treat the critical tissue more precisely.
This prospective, multi-center, single-blind, randomized controlled trial is testing whether adding LGE-MRI guidance to conventional electrical mapping improves the outcomes of VT ablation. Adults aged 18 to 75 years with structural heart disease and documented sustained VT will undergo cardiac MRI screening. Those with visible scar (LGE-positive) will be randomly assigned in a 1:1 ratio to one of two groups: ablation guided by LGE-MRI integrated with electroanatomical mapping (experimental group), or ablation guided by electroanatomical mapping alone without image integration (control group, with operators blinded to the MRI findings). Patients without scar on MRI will be followed in a separate observational registry.
All participants will be monitored in hospital for at least 24 hours after the procedure and will attend clinic visits at 3, 6, and 12 months. VT recurrence will be monitored with wearable smart ECG devices (worn for at least 7 days at each follow-up) and, in patients with an implantable cardioverter-defibrillator (ICD), by device interrogation. The main goal of the study is to determine whether MRI-guided ablation reduces the combined risk of VT recurrence, cardiovascular hospitalization, or death during 12 months of follow-up compared with standard ablation. The study also assesses procedure-related complications.
The 2 groups in the trial
- LGE-MRI-integrated EAM-guided ablationTreatment being tested
Patients undergo catheter ablation guided by integration of pre-procedural LGE-MRI scar imaging (ADAS-3D reconstruction) with electroanatomical mapping. In addition to conventional EAM-guided ablation, radiofrequency energy is delivered at the entrances of heterogeneous tissue channels identified on pixel signal intensity maps, regardless of local electrogram characteristics.
Treatment: LGE-MRI-integrated EAM-guided catheter ablation
- Conventional EAM-guided ablationExisting treatment, for comparison
Patients undergo catheter ablation guided by conventional three-dimensional electroanatomical mapping alone, without MRI image integration. Operators/mappers are blinded to the LGE-MRI findings.
Treatment: Conventional EAM-guided catheter ablation
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- Efficacy and Safety of MRI-guided Ventricular Tachycardia Ablation in Patients With Structural Heart Disease: A Randomized Controlled Trial.
- Fit questions
- Built from NCT07896980, who can take part
- Record updated
- 27 October 2026