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临床试验/NCT01310907
NCT01310907Unknown不适用

Identify the Genes Polymorphisms Related to Non-familial Bradyarrhythmia

China Medical University Hospital1 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2011年2月最近更新:
适应症

试验速览

阶段
不适用
入组人数
400
试验地点
1

研究概览

简要总结

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.

研究设计

研究类型
Observational

入排标准

性别
All
接受健康志愿者

入选标准

  • The patients with non-familial bradyarrhythmia

排除标准

  • Familial bradyarrhythmia Reversible bradyarrhythmia Bradyarrhythmia after open heart surgery and severe organic heart diseases

研究者

申办方类型
Other

研究点 (1)

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