Scar-related Atrial Tachycardia research hub
6 indexed studies · 5 currently recruiting
- recruitingNA
A Study Assessing Arrhythmia Mapping With a Multi-Electrode Mapping Catheter
This study is looking at a new, special device to help doctors understand heart rhythm problems. It aims to see if this device, a 'mapping catheter', is safe and works well to find where irregular heartbeats are coming from in the upper (atria) and lower (ventricles) chambers of the heart.
Belgium · France · Lithuania - recruiting
Clinical Course Of Disease In Participants With FA-CM
This study looks at how a heart condition linked to Friedreich Ataxia (FA-CM) changes over time. It aims to understand how the heart gets worse and could lead to new gene therapy treatments in the future for people with FA-CM.
United States · Brazil · Canada - ongoing, recruitingTherapeutic confirmatory (Phase III)
The efficacy and safety of Metoprolol as add-on treatment to standard of care in preventing cardiomyopathy in patients with Duchenne Muscular Dystrophy aged 8-17 years. A randomized, double-blind, placebo controlled study
This study looks at whether a medicine called Metoprolol can help prevent heart problems in young people with Duchenne Muscular Dystrophy. It compares Metoprolol to a dummy medicine to see if it makes a difference to heart strength.
Poland - enrolling by invitation
IVTCC 2.0: A Prospective Multicenter Ventricular Tachycardia Catheter Ablation Registry
This study is gathering information from people having a procedure called catheter ablation for fast heart rhythms like ventricular tachycardia or frequent extra heartbeats (PVCs). It aims to understand how well this treatment works and to improve care.
United States · Canada · Israel - recruiting
AIC Genotyping Study
This study looks at how certain gene changes might make some people with an irregular heartbeat (Atrial Fibrillation or AF) more likely to develop a weakened heart muscle (heart failure). We're comparing genes in different groups of people to understand this better.
United Kingdom - recruiting
Natural History Study in Pediatric Patients With MYBPC3 Mutation-associated Cardiomyopathy
This study looks at children and young people up to 18 with a heart condition called cardiomyopathy, caused by a gene change (MYBPC3 mutation). Researchers want to understand how the condition develops, its impact on life, and treatment options. It involves collecting information from their medical records.
United States · Canada · Spain