Actively Recruiting
Pre-warning Risk Scoring System for Sudden Cardiac Death
Led by Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University · Updated on 2024-06-05
100000
Participants Needed
1
Research Sites
252 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this observational study is to identify potential indicators for pre-warning of sudden cardiac death (SCD), including clinical biochemistry markers, electrocardiogram, echocardiography, MRI and CT imaging values, genetic markers and so on, and further construct a series of multi-parameter assessments of SCD early screening.
CONDITIONS
Official Title
Pre-warning Risk Scoring System for Sudden Cardiac Death
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with one or more cardiovascular diseases, including coronary heart disease, heart failure, or genetically related cardiomyopathy or arrhythmias
- History or new diagnosis of coronary heart disease or coronary angiography showing at least one vessel with >50% stenosis
- Heart failure diagnosis including reduced, intermediate, or preserved ejection fraction with evidence of increased left ventricular filling pressure
- Diagnosed with hypertrophic, dilated, arrhythmogenic right ventricular, or inflammatory cardiomyopathy, or hereditary arrhythmias such as long QT syndrome or Brugada syndrome
- Signed informed consent form
You will not qualify if you...
- Younger than 16 years old
- Refusal to attend follow-up visits
- Severe mental disorders preventing expression of wishes
- Presence of other serious physical diseases or abnormal laboratory test results
- Deemed unsuitable for participation by the supervising physician
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Sun Yat-sen Memorial Hospital of Sun Yat-sen University
Guanzhou, Guangdong, China, 510120
Actively Recruiting
Research Team
Y
Yuling Zhang, M.D.,Ph.D.
CONTACT
M
Maohuan Lin, M.D.,Ph.D.
CONTACT
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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