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Study identifier: NCT05556369 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Genetic Characterization of Cardiomyopathies (POLICARDIOMIO2021)

Condition: Cardiomyopathies  ·  Sponsor: Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

PhaseN/A
Planned participants288
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

Cardiomyopathy refers to a diverse group of myocardial diseases with multiple causes. In 1995, the World Health Organization classified cardiomyopathies into hypertrophic, dilated, restrictive, and mixed type. This classification is based on the pathophysiology of the disease. However, with rapid evolution of molecular genetics in cardiology, the American Heart Association in 2006 has classified cardiomyopathies into two major groups based on predominant organ involvement and etiology; Primary cardiomyopathies are those solely or predominantly confined to heart muscle and are relatively few in number. Secondary cardiomyopathies show pathologic myocardial involvement as part of a large number and variety of generalized systemic (multiorgan) disorders.Current evidence supports the use of genetic testing in clinical practice to improve risk stratification for clinically affected patients and their at-risk relatives for cardiomyopathies.

This description comes directly from the study's public registry record.

Talk to the study team

Stefano Carugo, Principal Investigator  ·  +39 0255033579  ·  stefano.carugo@policlinico.mi.it

Always discuss trial participation with your own doctor first.

Locations (1)

Fondazione IRCCS Ca' Granda, Ospedale Maggiore PoliclinicoMilan, Lombardy, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT05556369