Pediatric Cardiomyopathy Mutation Analysis

Recruiting now

Conditions studied: Cardiomyopathies, Dilated Cardiomyopathy, Hypertrophic Cardiomyopathy, Restrictive Cardiomyopathy, Arrhythmogenic Right Ventricular Cardiomyopathy, Left Ventricular Non-compaction Cardiomyopathy

In brief

The goal of this protocol is to obtain information from individuals with cardiomyopathy and from their families in order to elucidate the molecular genetics of this disorder. This will provide the basis for future genetic counseling as well as contribute to elucidating the biology of normal and abnormal cardiac function.

Key facts

Study ID

NCT02432092

Run by

Indiana University

People needed

300

Starts

2014-04-01

Expected to finish

2030-12-31

Last updated by the study team

2026-06-22

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects with cardiomyopathy
• Family members of subjects with cardiomyopathy

You may not qualify if…

• Subjects without cardiomyopathy
• Family members of subjects without cardiomyopathy

Full record on ClinicalTrials.gov

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