Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
600 participants
OBSERVATIONAL
2017-05-25
2022-05-31
Brief Summary
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Detailed Description
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Patients will be identified through the VA inpatient and outpatient clinic, and will be approached for inclusion in the study. The target enrollment for the research and biorepository is 600 participants. A detailed family history, medical background, study questionnaires and a blood sample will then be obtained by the principal investigator or a research coordinator, following written informed consent under a protocol approved by the Jesse Brown VA Institutional Review Board. Once enough samples are collected, coded DNA samples will be sent out to analyze for linkage to known/candidate loci for AF.
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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atrial fibrillation
Patients with a diagnosis of atrial fibrillation will be eligible for enrollment
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Subjects must have a documented history of atrial fibrillation by ECG, ECHO, and or Holter monitor event recorder.
* Subjects must be willing to give written, informed consent.
Exclusion Criteria
* Subjects who cannot speak English will be excluded from the study.
18 Years
100 Years
ALL
No
Sponsors
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Jesse Brown VA Medical Center
FED
Responsible Party
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Katherine Durham MS, APN
Cardiology Nurse Practitioner
Locations
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Jesse Brown VA Medical Center
Chicago, Illinois, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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977544
Identifier Type: -
Identifier Source: org_study_id
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