The Genetics of Cardiomyopathy and Heart Failure

Withdrawn before enrolling

Conditions studied: Dilated Cardiomyopathy, Hypertrophic Cardiomyopathy, Mitochondrial Cardiomyopathy, Noncompaction Cardiomyopathy, Restrictive Cardiomyopathy

In brief

The purpose of this study is to determine the genetic basis of cardiomyopathies and heart failure.

Key facts

Study ID

NCT00703443

Run by

University of California, Irvine

People needed

0

Starts

2007-04-01

Expected to finish

2007-04-01

Last updated by the study team

2021-01-25

Who can join

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

You may qualify if…

• Individuals with a diagnosis of cardiomyopathy
• Family members of individuals with a diagnosis of cardiomyopathy
• Individuals with a nuclear mutation shown to confer risk of cardiomyopathy but who do not themselves have cardiomyopathy

You may not qualify if…

• Individuals who do not have cardiomyopathy, a relative with cardiomyopathy, or a nuclear mutation predisposing to cardiomyopathy

Where it is running

• University of California, Irvine — Irvine, California, United States

Full record on ClinicalTrials.gov

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