Investigation of Genetic Risk of Atrial Fibrillation

Status Recruiting

Clinical Trial Summary

The atrial fibrillation (AF) is the most common cardiac rhythm disturbance that is responsible for substantial morbidity and mortality independent of associated heart disease or other risk factors. Even in the absence of preexisting cardiovascular disease, AF remains significantly associated with excess mortality rates. The current unsatisfactory treatment for AF comes from lack of understanding of the pathophysiology of AF. The purpose of this study is to identify gene polymorphisms that confer susceptibility to atrial fibrillation. Patients with AF（N=500） and healthy volunteer（N=1000） without AF are enrolled in this study. Patients with coronary artery disease, severe valvular heart disease, cardiomyopathy or heart failure were excluded from the study.

Clinical Trial Description

n/a

Study Design

Observational Model: Case Control, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Atrial Fibrillation

Clinical Trial Details

NCT number	NCT00412438
Study type	Observational
Source	Nagoya University
Contact	Kenji Yasui, MD, PhD
Phone	+81-52-788-6211
Email	kenji@riem.nagoya-u.ac.jp
Status	Recruiting
Phase	N/A
Start date	October 2006

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