Exome Sequencing Study in Cardiomyopathy to Identify New Risk Variants

Status Recruiting

Clinical Trial Summary

Genetic mutations has been proved to be associated wth the onset of cardiomyopathy. In the present study, we intend to identify new related variants or genes. From March, 2003 to November, 2017, patients diagnosed as cardiomyopathy were consecutively recruited, and their sampled were drawn from peripheral blood. Paired control group were also enrolled. The whole exome sequencing was used to find out the variants associated with the onset of cardiomyopathy and its prognosis.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03754101
Study type	Observational
Source	Tongji Hospital
Contact	Chenze Li, MD candidate
Phone	86-27-83663280
Email	lichenze@126.com
Status	Recruiting
Phase
Start date	March 3, 2003
Completion date	October 31, 2025

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