Actively Recruiting
Cohort Study of Chronic Heart Failure
Led by Jiangsu Taizhou People's Hospital · Updated on 2025-05-31
1000
Participants Needed
1
Research Sites
181 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this observational study is to learn about the influencing factors of chronic heart failure prognosis in heart failure patients. The main question it aims to answer is that what are the influencing factors of clinical outcomes in chronic heart failure. Participants will be collected multiple omics data such as phenotype group, environmental exposure group, intestinal microbiome, genome, metabolome, and noninvasive biomarkers.
CONDITIONS
Official Title
Cohort Study of Chronic Heart Failure
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- History of chronic heart failure or new-onset heart failure with specific heart function measures
- Diagnosed with dilated cardiomyopathy, hypertensive heart disease, ischemic cardiomyopathy, or non-severe valvular heart disease
- Receiving oral medication as primary post-discharge therapy
- Able to sign the informed consent form
You will not qualify if you...
- Renal failure with creatinine clearance less than 30 ml/min or dialysis treatment
- Correctable secondary causes of cardiac insufficiency including hyperthyroid heart disease, anemic heart disease, uncorrected congenital heart disease
- Severe valvular heart disease including severe aortic and mitral valve stenosis or closure
- Indications for pacemaker implantation without having received one
- Chronic obstructive pulmonary disease with type II respiratory failure
- Unable to understand or sign informed consent
- Mental illness, pregnancy, or other special populations
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Taizhou People's Hospital affiliated to Nanjing Medical University
Taizhou, Jiangsu, China, 225300
Actively Recruiting
Research Team
Y
Yucheng Wu, Doctor
CONTACT
L
Lichun Wang, Master
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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