Construction of a Cohort for Pan-Vascular Disease Among Employees of Taizhou People's Hospital
- Sponsor
- Jiangsu Taizhou People's Hospital
- Study ID
- NCT06545799
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
- Cardiovascular Death
- Myocardial Infarction
- Stroke
Eligibility Criteria
- Sex
- ALL
- Age
- 45 Years - N/A
- Healthy Volunteers
- Accepted
Study Details
1. Participant Recruitment During the annual health check-ups for hospital staff, potential participants are recruited. Those who express interest are provided with a detailed explanation of the study's objectives, content, and procedures, and are required to sign an informed consent form. 2. Screening Phase Medical history is collected, including any previous occurrences of myocardial infarction, ischemic or hemorrhagic stroke, or history of coronary, carotid, or peripheral arterial revascularization. 3. Baseline Data Collection 1\. Health Questionnaire Survey: Collect demographic information, medical history, and data on nutrition, physical activity, and smoking habits through a questionnaire. 2\. Clinical Assessments: Conduct the following assessments for all enrolled participants: * High-sensitivity cardiac troponin I and NT-proBNP testing * Non-invasive arterial stiffness testing * Measurement of visceral and subcutaneous fat content * Fundus photography * Body composition analysis 4 Regular Follow-Up Annual follow-up for a total of 10 years. The follow-up includes: 1. . Collection of updated demographic information and medical history, as well as repeated questionnaires on nutrition, physical activity, and smoking habits. 2. . Reassessment of the following items: * High-sensitivity cardiac troponin I and NT-proBNP testing * Non-invasive arterial stiffness testing * Measurement of visceral and subcutaneous fat content * Fundus photography * Body composition analysis 5 Outcome Evaluation 1). Primary Outcomes: Cardiovascular mortality, non-fatal myocardial infarction, or non-fatal stroke events. 2). Secondary Outcomes: All vascular events, changes in cardiovascular biomarkers, and degree of arterial stiffness.
Key Dates
- First listed
- Aug 9, 2024
- Start date
- Sep 1, 2024
- Status verified
- Aug 2024
- Primary completion
- Sep 1, 2034
- Completion
- Sep 1, 2034
Study Design
- Enrollment
- 1,000 participants (estimated)
Primary Outcome Measure
Cardiovascular death, non-fatal myocardial infarction, or non-fatal stroke events [ Time Frame: September 2024 to August 2034 ]
Central Contacts
- Qingqing Zhang+86 180 6198 6120
Find similar trials
Related Studies
- Evaluation of an Advanced Lower Extremity NeuroprosthesesRecruiting · Case Western Reserve University · Cleveland, Ohio
- Genetic and Environmental Risk Factors for Hemorrhagic StrokeRecruiting · State University of New York at Buffalo · Chicago, Illinois
- Circulating Markers for Ischemic Heart DiseaseRecruiting · UConn Health · Farmington, Connecticut
- Identification of Genomic Predictors of Adverse Events After Cardiac SurgeryRecruiting · Brigham and Women's Hospital · Dallas, Texas