Identification of Genetic, Biochemical and Hormonal Factors Contributing to Atrial Fibrillation
1 other identifier
observational
1,300
1 country
1
Brief Summary
The purpose of this study is to establish a genebank repository of blood samples and data to generate information about the hereditary (genetic) basis of atrial fibrillation.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2005
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2005
CompletedFirst Submitted
Initial submission to the registry
January 10, 2008
CompletedFirst Posted
Study publicly available on registry
January 23, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2035
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2035
September 10, 2025
August 1, 2025
30.4 years
January 10, 2008
September 8, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Genetic variants associated with atrial fibrillation
Genome-wide association study of atrial fibrillation
Baseline
Study Arms (2)
atrial fibrillation
Atrial fibrillation
Control
Control subjects with no atrial fibrillation
Eligibility Criteria
Subjects with atrial fibrillation
You may qualify if:
- Male or female at least 18 years old
- Subjects with a history of or current Atrial Fibrillation
You may not qualify if:
- Male or female at least 18 years old
- Subjects with no history of Atrial Fibrillation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cleveland Clinical Foundation
Cleveland, Ohio, 44145, United States
Biospecimen
plasma, serum, buffy coat, DNA
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Mina K Chung, MD
The Cleveland Clinic
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
January 10, 2008
First Posted
January 23, 2008
Study Start
August 1, 2005
Primary Completion (Estimated)
December 1, 2035
Study Completion (Estimated)
December 1, 2035
Last Updated
September 10, 2025
Record last verified: 2025-08
Data Sharing
- IPD Sharing
- Will not share