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