Viewing Study NCT00138931



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Last Modification Date: 2024-10-26 @ 9:14 AM
Study NCT ID: NCT00138931
Status: RECRUITING
Last Update Posted: 2023-05-06
First Post: 2005-08-29

Brief Title: Genetics of Cardiovascular and Neuromuscular Disease
Sponsor: University of Chicago
Organization: University of Chicago

Study Overview

Official Title: Genetic Studies of Patients and Their Families With Inherited Cardiovascular and Neuromuscular Diseases
Status: RECRUITING
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None