NCT00921986

Brief Summary

Biorepository of blood and or tissue samples from patients presenting with cardiac arrhythmia syndromes.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,000

participants targeted

Target at P75+ for all trials

Timeline
117mo left

Started Mar 2009

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress64%
Mar 2009Dec 2035

Study Start

First participant enrolled

March 1, 2009

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

June 15, 2009

Completed
2 days until next milestone

First Posted

Study publicly available on registry

June 17, 2009

Completed
26.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2035

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2035

Last Updated

September 10, 2025

Status Verified

August 1, 2025

Enrollment Period

26.8 years

First QC Date

June 15, 2009

Last Update Submit

September 8, 2025

Conditions

Keywords

geneticsbiorepositorycardiac deathatrial fibrillationventricular fibrillationventricular tachycardiasupraventricular tachycardiaspremature ventricular complexespremature atrial complexesatrioventricular and intraventricular blockssinus node dysfunctionsyncopevasovagal reactivitypostural orthostatic tachycardia syndrome

Outcome Measures

Primary Outcomes (1)

  • Genetic variants associated with arrhythmias

    Genome-wide association study of arrhythmias

    Baseline

Study Arms (2)

Arrhythmias

Patients with arrhythmias

Control Subjects

Subjects that do not have a history of cardiac arrhythmias.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients undergoing arrhythmia procedures, cardiac surgery or inpatient or outpatient evaluations for arrhythmias at the Cleveland Clinic or from outside collaborative institutions or from other clinical trials.

You may qualify if:

  • Male or female at least 18 years old
  • Subjects with a history of or current cardiac arrhythmia, family members of subjects with cardiac arrhythmias, or no cardiac arrhythmia if a Control Subject.

You may not qualify if:

  • Subjects previously enrolled in the Arrhythmia BioBank

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cleveland Clinic Foundation

Cleveland, Ohio, 44195, United States

RECRUITING

Biospecimen

Retention: SAMPLES WITH DNA

Biospecimens to be collected: DNA, RNA, plasma, \& serum. Also tissue may be collected.

MeSH Terms

Conditions

Arrhythmias, CardiacDeathAtrial FibrillationVentricular FibrillationTachycardia, VentricularTachycardia, SupraventricularVentricular Premature ComplexesAtrial Premature ComplexesSick Sinus SyndromeSyncopePostural Orthostatic Tachycardia Syndrome

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular DiseasesPathologic ProcessesPathological Conditions, Signs and SymptomsTachycardiaCardiac Conduction System DiseaseCardiac Complexes, PrematureArrhythmia, SinusHeart BlockUnconsciousnessConsciousness DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsOrthostatic IntolerancePrimary DysautonomiasAutonomic Nervous System Diseases

Study Officials

  • Mina K. Chung, MD

    The Cleveland Clinic

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Mina K. Chung, MD

CONTACT

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

June 15, 2009

First Posted

June 17, 2009

Study Start

March 1, 2009

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

Locations