Actively Recruiting

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ID03821051

China Structural Ventricular Arrhythmias Registry, a Multicenter, Observational and Prospective Study

Led by China National Center for Cardiovascular Diseases · Updated on 2019-01-29

2000

Participants Needed

1

Research Sites

260 weeks

Total Duration

On this page

Sponsors

C

China National Center for Cardiovascular Diseases

Lead Sponsor

R

Renmin Hospital of Wuhan University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are conducting a prospective, observational study involving multiple centers in China to better understand malignant structural ventricular arrhythmias. The study aims to build a risk stratification model to identify risk factors and develop more efficient and cost-effective strategies for early prevention and treatment. This research is part of a larger national effort to clarify the prevalence and risk factors of this condition, which currently relies heavily on implantable devices and medication. The study will enroll 2000 participants diagnosed with ventricular arrhythmias caused by structural heart diseases such as ischemic cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, dilated cardiomyopathy, and hypertrophic cardiomyopathy. At enrollment, demographic information, medical history, clinical features, lab tests, imaging, medications, procedures, and in-hospital outcomes will be collected from medical records. Blood samples will also be taken to detect biological markers like genes and inflammatory factors. Participants will be followed up every six months to monitor arrhythmia status, medication use, and clinical events. Participants will undergo interviews and provide consent at the start of the study. During follow-up visits every six months, researchers will assess episodes of arrhythmia, sustained tachycardia or ventricular fibrillation, sudden cardiac death, and overall mortality over a five-year period. The study will gather comprehensive clinical and biological data to help improve risk prediction and management of ventricular arrhythmias. The total duration of participant involvement is expected to be five years, with continuous monitoring of health outcomes and events.

CONDITIONS

Brief Title

China Structural Ventricular Arrhythmias Registry

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with ventricular arrhythmia caused by structural heart diseases such as ischemic cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, dilated cardiomyopathy, or hypertrophic cardiomyopathy
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

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)

Monitoring

Duration - Up to 5 years

Participants are observed and followed to collect data on arrhythmia condition, medication use, clinical events, and other health information.

Visits every 6 months

Trial Site Locations

Total: 1 location

1

China National Center for Cardiovascular Diseases

Beijing, Beijing Municipality, China, 100037

Actively Recruiting

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Research Team

Y

Yan Yao, MD,PhD

S

Shangyu Liu, 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

0

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