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Identify the Genes Polymorphisms Related to Non-familial Bradyarrhythmia

NCT01310907 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 400

Last updated 2011-03-09

No results posted yet for this study

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.

Conditions

  • Bradyarrhythmia

Sponsors & Collaborators

  • China Medical University, China

    collaborator OTHER

  • China Medical University Hospital

    lead OTHER

Principal Investigators

  • Jan-Yow Chen, MD · China Medical University Hospital

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-02-28

Countries

  • Taiwan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01310907 on ClinicalTrials.gov