Identify the Genes Polymorphisms Related to Non-familial Bradyarrhythmia

Status Recruiting

Clinical Trial Summary

Bradyarrhythmia, including sinus node dysfunction and atrioventricular block, is a major cause necessitating pacemaker implantation. In contrast to familial bradyarrhythmia known as by mutations at particular ion channels, limited information is available for the mechanistic study in non-familial bradyarrhythmia.

Possible gene polymorphisms related to non-familial bradyarrhythmia were studied. Comparison of multi-locus analysis and single-locus analysis will be analyzed between the cases and controls. Functional studies will perform to clarify the results of association study.

Clinical Trial Description

n/a

Study Design

N/A

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01310907
Study type	Observational
Source	China Medical University Hospital
Contact	Jan-Yow Chen, MD
Phone	+422052121
Email	janyow@ms77.hinet.net
Status	Recruiting
Phase	N/A
Start date	February 2011

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