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NCT00921986 Clinical Trial

Biospecimen Repository for Cardiac Arrhythmias at the Cleveland Clinic

Arrhythmias, Cardiac Clinical Trial

Official title:
Cleveland Clinic Arrhythmia Biospecimen Repository (Cleveland Clinic Arrhythmia BioBank)

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00921986
Other study ID # 09-176
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 2009
Est. completion date December 2035

Study information
Verified date August 2023
Source The Cleveland Clinic
Contact Mina K. Chung, MD
Phone 216.444.2290
Email chungm@ccf.org
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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

Description:

The long-term objective of this research is to find genes and biologic pathways causing arrhythmia syndromes and other diseases or conditions. In order to achieve this objective the investigators will collect comprehensive phenotypic data and corresponding blood and/or tissue samples into a biorepository registry of patients, presenting for cardiac arrhythmia evaluation and/or treatment, and control subjects without arrhythmias. This biorepository will be composed of two parts: 1) An Arrhythmia Biorepository of blood and tissue from patients undergoing arrhythmia procedures, cardiac surgery, or inpatient or outpatient evaluations for arrhythmias, and 2) A Collaborative Sample Biorepository for de-identified samples and data from outside institutions and clinical trials.

Recruitment information / eligibility
Status Recruiting
Enrollment 2000
Est. completion date December 2035
Est. primary completion date December 2035
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 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. Exclusion Criteria: - Subjects previously enrolled in the Arrhythmia BioBank

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Cleveland Clinic Foundation Cleveland Ohio

Sponsors (1)
Lead Sponsor Collaborator
The Cleveland Clinic

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Genetic variants associated with arrhythmias Genome-wide association study of arrhythmias Baseline
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