Actively Recruiting
Real-Time Intracardiac Echocardiography for Ventricular Arrhythmia Ablation
Led by Insel Gruppe AG, University Hospital Bern · Updated on 2026-04-01
70
Participants Needed
2
Research Sites
66 weeks
Total Duration
On this page
Sponsors
I
Insel Gruppe AG, University Hospital Bern
Lead Sponsor
U
University of Bern
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study is investigating whether using ultrasound directly inside the heart during ablation of heart rhythm disorders in the ventricles can reduce radiation exposure for patients. During an ablation, catheters are guided through the heart to treat the abnormal electrical signals. Usually, X-ray imaging (fluoroscopy) is used to see where the catheters are, which exposes both patients and hospital staff to radiation. The study is randomized and controlled: half of the participants will have the ablation with ultrasound inside the heart, and the other half will have the standard ablation without ultrasound during the procedure. The main goal is to compare the amount of X-ray time used during the procedure. Secondary goals are to look at safety, effectiveness, and the total procedure time. Patients with premature ventricular contractions or ventricular tachycardia can take part. A total of 70 people will be included, 35 in each group. Using ultrasound inside the heart makes it possible to see the catheters and heart structures directly, so many steps can be done without X-rays. This could make ablations safer and reduce radiation exposure. The study is being carried out at Inselspital, Bern University Hospital, and at University Hospital Basel. All steps are standardized and data are collected carefully. The results will show whether ultrasound during ablations can significantly reduce radiation and make ablations more efficient and safer.
CONDITIONS
Official Title
Real-Time Intracardiac Echocardiography for Ventricular Arrhythmia Ablation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients 18 years or older undergoing a premature ventricular contraction or ventricular tachycardia ablation.
You will not qualify if you...
- Ventricular arrhythmia likely originating in the right ventricular outflow tract (left-bundle-inferior axis, >V4 precordial transition).
- Planned primary epicardial ablation.
- Presence of congenital heart disease.
- Presence of a mechanical tricuspid valve prosthesis.
- Unwilling or unable to fully comply with study procedures and follow-up.
AI-Screening
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Trial Site Locations
Total: 2 locations
1
University Hospital Basel
Basel, Switzerland, 4013
Actively Recruiting
2
Inselspital, Bern University Hospital
Bern, Switzerland, 3010
Actively Recruiting
Research Team
B
Boldizsar Kovacs, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
DIAGNOSTIC
Number of Arms
2
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