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Construction of a Cohort for Pan-Vascular Disease Among Employees of Taizhou People's Hospital

J

Jiangsu Taizhou People's Hospital

Status

Not yet enrolling

Conditions

Stroke
Cardiovascular Death
Myocardial Infarction

Study type

Observational

Funder types

Other

Identifiers

NCT06545799
KY 2024-098-01

Details and patient eligibility

About

  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

  4. Health Questionnaire Survey: Collect demographic information, medical history, and data on nutrition, physical activity, and smoking habits through a questionnaire.

  5. 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.

Enrollment

1,000 estimated patients

Sex

All

Ages

45+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Employed or retired individuals aged 45 years or older;
  2. Willing to sign an informed consent form and voluntarily participate in health examinations and related data collection.

Exclusion criteria

  1. History of myocardial infarction, ischemic or hemorrhagic stroke, or revascularization of coronary, carotid, or peripheral arteries;
  2. Employees with severe psychological disorders who are unable to cooperate with the study;
  3. Pregnant or breastfeeding women.

Trial contacts and locations

0

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Central trial contact

Qingqing Zhang

Data sourced from clinicaltrials.gov

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