Multi-ethnic dilated cardiomyopathy registry
Part of Genetic & congenital, Heart & circulation clinical trials.
This study is a registry for people with dilated cardiomyopathy (DCM)—a condition where the heart's main pumping chamber becomes enlarged and weak. It aims to learn more about DCM, especially in people from different ethnic backgrounds, by collecting health information over time.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You must be 18 years old or older.
- You must be a patient at a University of Illinois Hospital (UIH) site.
- You must be able to give your own permission (informed consent) to be in the study.
- You cannot be pregnant at the start of the study.
- You cannot be in prison.
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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