Beijing Vascular Disease Patients Evaluation STudy

NCT02569268 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2000

Last updated 2016-05-10

No results posted yet for this study

Summary

Arteriosclerotic vascular-related diseases have become a serious threat to human health. The prevention and reversal of vascular events has become an important direction of medicine. Early vascular disease detection system includes pulse wave velocity (PWV), carotid intima-media thickness (IMT) and coronary flow velocity reserve (CFVR), flow-mediated vasodilation (FMD), cardio-ankle vascular index (CAVI), ankle-brachial index (ABI), insulin resistance index (HOMA-IR), hypersensitivity C- reactive protein (hs-CRP), plasma homocysteine (Hcy), B-type natriuretic peptide (BNP), uric acid (UA), and so on. However, there is no international and domestic comprehensive study on simple and practical evaluation system by jointing application of these evaluation indexes to detect vascular disease. Combined evaluation function can simultaneously detect and evaluate vascular abnormalities, make up a single indicator shortcoming in clinical applications from multiple levels of vascular structure and function. However, all indicators testing not only cause time consuming, but also increase the burden on patients, resulting unnecessary waste of medical resources. Thus, the present study was to select appropriate indicators and effective joint, and establish the rating system, using the vascular system to predict the incidence of terminal events, and compare this system with the previous scoring system such as FRS (Framingham Risk Score) pros and cons.

Conditions

  • Vascular Disease

Interventions

OTHER

Questionnaires and follow-up

Detecting the vascular functional parameters, questionnaire and follow-up: For 2 years or the occurrence of vascular events end time, including cardiovascular events (acute myocardial infarction, angina, coronary reperfusion therapy), stroke, heart failure, peripheral vascular disease.

Sponsors & Collaborators

  • Peking University Third Hospital

    collaborator OTHER
  • Peking University Health Science Center

    collaborator OTHER
  • Beijing Municipal Science & Technology Commission

    collaborator OTHER
  • Chinese National Natural Science Foundation Commission

    collaborator UNKNOWN
  • Ministry of Education, China

    collaborator OTHER_GOV
  • National Health and Family Planning Commission of the China

    collaborator UNKNOWN
  • Peking University Shougang Hospital

    lead OTHER

Eligibility

Min Age
45 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-01-31
Primary Completion
2015-12-31
Completion
2015-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02569268 on ClinicalTrials.gov