Histiocytoid cardiomyopathy
MONDO:0010771Histiocytoid cardiomyopathy is an arrhythmogenic disorder characterized by cardiomegaly, severe cardiac arrhythmias or sudden death, and the presence of histiocyte-like cells within the myocardium.
Also known as: Arachnocytosis of the myocardium, Purkinje cell hamartoma, congenital cardiomyopathy, foamy myocardial transformation of infancy, histiocytoid cardiomyopathy, infantile cardiomyopathy with histiocytoid change, infantile xanthomatous cardiomyopathy, isolated Cardiac lipidosis
24 clinical trials for this condition and its sub-types, 3 tagged with Histiocytoid cardiomyopathy itself.
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Browse by category →Sub-types of Histiocytoid cardiomyopathy
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Cardiac lipidosis, familial 0 trials
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Baby brain waves may reveal future learning risks after heart surgery
Knowledge-focused Recruiting nowThis study looks at whether brain wave tests (EEG) done before and after heart surgery in babies under 1 year old can predict later learning or behavior problems, such as autism or ADHD. About 50 infants will be followed to age 2. The goal is to find early warning signs so that c…
Sponsor: University Hospital, Lille • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:23 UTC
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Smartwatch study aims to keep pregnant heart patients safer at home
Knowledge-focused Recruiting nowThis study tests whether a wrist-worn device can help monitor pregnant women with congenital heart disease. Researchers will track heart rhythms and other data from 50 participants to see if the wearable can detect early signs of trouble. The goal is to improve care and reduce th…
Sponsor: The Cleveland Clinic • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:04 UTC