Trials / Unknown
UnknownNCT01310907
Identify the Genes Polymorphisms Related to Non-familial Bradyarrhythmia
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 400 (estimated)
- Sponsor
- China Medical University Hospital · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Accepted
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
Timeline
- Start date
- 2011-02-01
- First posted
- 2011-03-09
- Last updated
- 2011-03-09
Locations
2 sites across 1 country: Taiwan
Source: ClinicalTrials.gov record NCT01310907. Inclusion in this directory is not an endorsement.