Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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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