Clinical Trial: Registry and Prevalence of Gene Mutation in Korean Patients With Familial Hypertrophic Cardiomyopathy

Study Status: Completed
Recruit Status: Completed
Study Type: Observational [Patient Registry]

Official Title:

Brief Summary: Set the Korean Familial Hypertrophic Cardiomyopathy (KFHC) registry to study the prevalence of gene mutations in Korean patients with familial hypertrophic cardiomyopathy

Detailed Summary:
Sponsor: Yonsei University

Current Primary Outcome: 1) DNA analysis [ Time Frame: 1 year ]

1) Identify susceptible genes for familial hypertrophic cardiomyopathy in Korean


Original Primary Outcome: Same as current

Current Secondary Outcome: 2) Prognosis of familial hypertrophic cariomyopathy [ Time Frame: 1 year ]

2) all-cause mortality, hospitalization for heart failure progression, stroke, heart transplantation


Original Secondary Outcome: Same as current

Information By: Yonsei University

Dates:
Date Received: February 7, 2013
Date Started: February 2013
Date Completion:
Last Updated: February 17, 2014
Last Verified: February 2014