Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID00921986

Cleveland Clinic Arrhythmia Biospecimen Repository for Cardiac Arrhythmias

Led by The Cleveland Clinic · Updated on 2025-09-10

2000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to identify genes and biological pathways that cause arrhythmia syndromes and related conditions. To support this, the study collects detailed health data and blood or tissue samples from patients undergoing evaluation or treatment for cardiac arrhythmias, as well as control subjects without arrhythmias. It includes a biorepository registry and a collaborative sample bank with de-identified samples from other institutions and trials. Participants are divided into two groups: those with arrhythmias and those without a history of cardiac arrhythmias serving as controls. Blood and tissue samples are collected from patients undergoing arrhythmia procedures, cardiac surgery, or evaluations. The study gathers both phenotypic data and biological samples to create a comprehensive resource for research. During the study, participants provide biological samples and clinical information, which are stored in the biorepository. Researchers analyze genetic variants associated with arrhythmias as a primary outcome. The study allows for long-term collection and use of these samples to better understand arrhythmia causes. Participation involves providing samples and data, with follow-up as needed, and the study is open to adults aged 18 and older.

CONDITIONS

Brief Title

Biospecimen Repository for Cardiac Arrhythmias at the Cleveland Clinic

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female at least 18 years old
  • Subjects with a history of or current cardiac arrhythmia
  • Family members of subjects with cardiac arrhythmias
  • Control subjects without cardiac arrhythmia
Not Eligible

You will not qualify if you...

  • Previously enrolled in the Arrhythmia BioBank study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Sample Collection

Duration - Ongoing throughout the study period

Participants undergo collection of blood and/or tissue samples and comprehensive phenotypic data for the biorepository.

1 to multiple visits depending on procedures and participant group

Long-term Monitoring

Duration - Up to 2035-12

Participants are observed over time to collect data related to cardiac arrhythmias and related conditions.

Visits as scheduled based on clinical evaluations

Trial Site Locations

Total: 1 location

1

Cleveland Clinic Foundation

Cleveland, Ohio, United States, 44195

Actively Recruiting

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Research Team

M

Mina K. Chung, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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