Atrial fibrillation, familial, 13
MONDO:0014155Any familial atrial fibrillation in which the cause of the disease is a mutation in the SCN1B gene.
Also known as: SCN1B familial atrial fibrillation, atrial fibrillation, familial, 13, atrial fibrillation, familial, type 13, familial atrial fibrillation caused by mutation in SCN1B, ATFB13
30 clinical trials for this condition and its sub-types, 0 tagged with Atrial fibrillation, familial, 13 itself.
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Massive heart study aims to sharpen diagnosis and cut needless hospital stays
Knowledge-focused Not yet recruitingThis study follows 25,000 people referred to a specialized heart clinic with symptoms like chest pain or shortness of breath. Researchers will track which heart conditions are actually diagnosed and how patients are evaluated. The goal is to improve diagnostic accuracy and unders…
Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Knowledge-focused
Last updated Jul 02, 2026 00:00 UTC
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AI could predict strokes before they happen in heart patients
Knowledge-focused Not yet recruitingThis study will test whether an artificial intelligence (AI) tool can better predict stroke risk in 1,000 people aged 65-95 with atrial fibrillation, compared to current methods. The AI analyzes health records and heart data to identify high-risk individuals early. The goal is to…
Sponsor: Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:09 UTC
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Could heart and muscle disorders share a genetic cause?
Knowledge-focused Not yet recruitingThis study looks at whether people with certain heart rhythm disorders also carry genetic variants linked to a rare muscle condition called non-dystrophic myotonia. Researchers will review medical records of 570 participants and invite some for a neurological exam and electromyog…
Sponsor: Universitair Ziekenhuis Brussel • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:00 UTC