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RECRUITING
NCT00138931

Genetics of Cardiovascular and Neuromuscular Disease

Sponsor: University of Chicago

View on ClinicalTrials.gov

Summary

We are studying the genetics of human cardiovascular and neuromuscular disease. There are many different genetic regions that have been associated with the development of cardiomyopathy. An equal number of genetic regions have been associated with muscular dystrophy and there is overlap because some of the identical genes, when mutated, produce both cardiomyopathy and muscular dystrophy. We are working to identify genes and gene mutations associated with cardiomyopathy, arrhythmias and muscular dystrophy. We propose to screen these samples for mutations in genes known to be involved in these disorders.

Official title: Genetic Studies of Patients and Their Families With Inherited Cardiovascular and Neuromuscular Diseases.

Key Details

Gender

All

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

2000

Start Date

1996-09

Completion Date

2030-01

Last Updated

2025-09-09

Healthy Volunteers

No

Interventions

PROCEDURE

Blood draw (genetic testing)

Blood draw (genetic testing)

Locations (1)

University of Chicago

Chicago, Illinois, United States