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Clinical Trials in China / NCT07151183
Recruiting Observational

Diagnosis, Prognosis, and Mechanisms in Panvascular Disease

NCT07151183 · tracked via the Priya Life Science China tracker
Sponsor
Jinwei Tian
Phase
Observational
Started
2024-12-01
Last updated
2025-09-03

Condition(s) studied

Panvascular DiseasesCardiovascular Diseases

Investigational drug(s) / intervention(s)

No intervention

No intervention: No intervention

Study summary

This study aims to establish a standardized cohort for panvascular diseases, encompassing biological materials such as DNA samples, along with extensive patient medical records and follow-up information. The design of this database will enable it to serve as a comprehensive resource for future medical research.

Upon data collection, researchers will conduct various statistical analyses to enhance our understanding of the factors and mechanisms contributing to various panvascular diseases, including coronary heart disease, myocardial infarction, stroke, and peripheral vascular disease. These statistical analyses will also aid in identifying more effective treatment strategies for these conditions.

By amassing a large volume of data from a significant number of patients with panvascular diseases, researchers will be able to perform highly precise analyses of the factors influencing the onset, progression, and treatment of these diseases. The results of these precise analyses can then be utilized to optimize clinical practices for the prevention and treatment of panvascular diseases.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. Male or female aged 18 to 80 years old; 2. Diagnosed or suspected panvascular disease, defined as the presence of atherosclerotic lesions in at least two or more vascular regions, such as intracranial arteries, carotid arteries, coronary arteries, aorta, and peripheral arteries; 3. Voluntary participation in this study and provision of signed informed consent. Exclusion Criteria: 1. Severe hemodynamic instability; 2. Severe cardiac dysfunction (EF \< 30%); 3. Severe arrhythmias; 4. Severe valvular heart disease; 5. Cardiomyopathy caused by non-coronary artery diseases; 6. Non-atherosclerotic coronary artery disease (e.g., coronary artery dissection, embolism, etc.); 7. Severe non-cardiovascular diseases; 8. Women who are pregnant or breastfeeding; 9. Individuals who refuse to provide signed informed consent.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Harbin Medical University Harbin Heilongjiang Recruiting

More Jinwei Tian trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07151183 on ClinicalTrials.gov ↗ ← All trials in China