Skip to content

Clinical Outcomes of Cardiovascular Disease

Clinical Outcomes of Cardiovascular Disease: a Prospective Cohort Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06459934
Acronym
CLEAR
Enrollment
30000
Registered
2024-06-14
Start date
2024-06-01
Completion date
2028-12-31
Last updated
2024-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Diseases, Coronary Artery Disease, Heart Failure

Brief summary

This study is a prospective, single center cohort study that primarily registers the clinical characteristics, outcomes, and influencing factors of patients with different types of cardiovascular diseases. Evaluate multiple examination indicators of patients at baseline, 1 year and longer, and follow up on the incidence of major cardiovascular and cerebrovascular adverse events, heart failure readmission, death, and other endpoint events.

Detailed description

This study is a prospective, single center cohort study that primarily registers the clinical characteristics, outcomes, and influencing factors of patients with different types of cardiovascular diseases. Mainly including coronary heart disease, cardiomyopathy, hypertension, heart failure and other diseases, multiple examination indicators are evaluated for patients at baseline, 1 year and longer periods of time. The primary endpoints for coronary heart disease are all-cause mortality, cardiogenic death, non fatal myocardial infarction, hospitalization for heart failure, and major cardiovascular adverse events. The primary endpoints for cardiomyopathy are all-cause mortality, cardiogenic death, hospitalization for heart failure, and major cardiovascular adverse events. The primary endpoints for hypertension are stroke, all-cause mortality, cardiogenic death, hospitalization for heart failure, and major cardiovascular and cerebrovascular adverse events. The primary endpoints for heart failure are all-cause mortality, cardiogenic death, readmission for heart failure, and major cardiovascular adverse events.

Interventions

None listed

Sponsors

Xinjiang Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Coronary heart disease According to coronary angiography and coronary CTA, at least one coronary artery has a degree of stenosis greater than 50%. 2. Hypertension Hypertension is defined as office systolic blood pressure is ≥ 140mmHg and/or the diastolic blood pressure is ≥ 90mmHg without the use of antihypertensive drugs. 3. Heart failure There is a clear history of organic heart disease, clinical symptoms and signs of heart failure, and objective evidence of heart failure. 4. Cardiomyopathy Including defined dilated cardiomyopathy, hypertrophic cardiomyopathy, restrictive cardiomyopathy, etc. 5. Able to sign informed consent form.

Exclusion criteria

1. Age\<18 years old, or\>80 years old. 2. Patients with various malignant tumors. 3. Liver dysfunction (defined as ALT or total bilirubin greater than three times the upper normal limit). 4. Renal insufficiency (defined as blood creatinine exceeding 1.5 times the upper normal limit). 5. Those who have participated in other clinical studies within the past three months. 6. Individuals without legal capacity or with limited legal capacity. 7. Any situation where the researcher deems it unsuitable to participate in the clinical study.

Design outcomes

Primary

MeasureTime frameDescription
All cause death1 year.Death caused by various reasons.
Cardiac death1 year.Death caused by cardiac reasons.
Main adverse cardiovascular events(MACE)1 year.The composite endpoint for hospitalization for heart failure, non fatal myocardial infarction, and cardiac death.
Heart failure1 year.Heart failure (HF) is defined according to the diagnostic criteria for HF. Briefly, HF was defined as typical signs and symptoms of HF (NYHA class III or IV), as well as a history of myocardial infarct (MI) or with advanced coronary artery disease including severe 3-vessel disease and chronic total occlusion or other Organic heart disease.
Stroke1 year.Stroke was defined as a sudden onset of vertigo, numbness, aphasia, or dysarthria caused by cerebrovascular disease, including hemorrhage, embolism, thrombosis, or aneurysm rupture, and persisting for \> 24 hours

Secondary

MeasureTime frameDescription
Stroke3 years.Stroke was defined as a sudden onset of vertigo, numbness, aphasia, or dysarthria caused by cerebrovascular disease, including hemorrhage, embolism, thrombosis, or aneurysm rupture, and persisting for \> 24 hours
Heart failure3 years.Heart failure (HF) is defined according to the diagnostic criteria for HF. Briefly, HF was defined as typical signs and symptoms of HF (NYHA class III or IV), as well as a history of myocardial infarct (MI) or with advanced coronary artery disease including severe 3-vessel disease and chronic total occlusion or other Organic heart disease.
Main adverse cardiovascular and cerebrovascular events(MACCE)1 year.The composite endpoint for hospitalization for heart failure, non fatal myocardial infarction, cardiac death, and stroke.
All cause death3 years.Death caused by various reasons.
Cardiac death3 years.Death caused by cardiac reasons.
Main adverse cardiovascular events(MACE)3 years.The composite endpoint for hospitalization for heart failure, non fatal myocardial infarction, and cardiac death.

Countries

China

Contacts

Primary ContactYing-Ying Zheng, PhD
zhengying527@163.com+8615214804944

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026