Hospital Sant Joan de Déu Barcelona

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Natural History Study in Pediatric Patients With MYBPC3 Mutation-associated Cardiomyopathy	Cardiomegaly, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, aortic valve disorder, aortic valve stenosis, cardiomyopathy, cardiovascular disorder, dilated cardiomyopathy, heart disorder, heart valve disorder, hereditary disease, hypertrophic cardiomyopathy, laminopathy, restrictive cardiomyopathy, subvalvular aortic stenosis	Active, not recruiting	Not stated	2026-09-02		NCT05112237

Clinical trials