Scientists probe why heart treatments fail in common genetic condition
NCT ID NCT07454135
Summary
This study aims to understand why a type of irregular heartbeat (atrial fibrillation) is more common and harder to treat in people with a genetic condition that causes thickened heart muscle (hypertrophic cardiomyopathy). Researchers will study 40 adults with both conditions using heart scans and electrical signal measurements during a planned treatment procedure. The goal is to gather knowledge that could lead to better future treatments for this specific group of patients.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes NO responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for ATRIAL FIBRILLATION (AF) are added.
By submitting, you agree to our Terms of use
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Locations
-
Guy's and St Thomas' NHS Foundation Trust
London, United Kingdom
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
Explore the condition pages connected to this study.