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Clinical Trials/NCT04253054
NCT04253054UnknownNot Applicable

Chinese Multi-provincial Cohort Study-Beijing Project

Beijing Institute of Heart, Lung and Blood Vessel Diseases3 sites in 1 country3,000 target enrollmentStarted: September 7, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
3,000
Locations
3
Primary Endpoint
All fatal and nonfatal acute coronary and stroke events

Study Overview

Brief Summary

The Chinese Multi-provincial Cohort Study (CMCS)-Beijing project is a sub-study in CMCS participants from Beijing, which intended to investigate the progression and determinants of atherosclerosis and aging related health problems through repeat examinations. Exam 0 to Exam 3 have been conducted during 1992 to 2012. Exam 4 is scheduled in 2020.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
60 Years to 100 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Participants from CMCS-Beijing
  • sign the informed consent

Exclusion Criteria

  • participanting in clinical trials

Outcomes

Primary Outcomes

All fatal and nonfatal acute coronary and stroke events

Time Frame: From date of enrollment until the date of first documented event or date of cardiovascular death, whichever came first, assessed at least 5 years

Acute coronary heart disease events included acute myocardial infarction, sudden death, and other coronary deaths. Acute stroke events included subarachnoid hemorrhage, intracerebral hemorrhage, or cerebral infarction.

Secondary Outcomes

  • Cognitive dysfunction(From date of enrollment until date of first documented event, assessed at least 5 years)
  • Valvular disease(From date of enrollment until the date of first documented event or date of valvular disease death, whichever came first, assessed at least 5 years)
  • New-onset of stroke(From date of enrollment until the date of first documented event or date of stroke death, whichever came first, assessed at least 5 years)
  • Total death(From date of enrollment until date of death from all cause, assessed at least 5 years)
  • Olfactory Disorders(From date of enrollment until date of first documented event, assessed at least 5 years)
  • New-onset of coronary events(From date of enrollment until the date of first documented event or date of CHD death, whichever came first, assessed at least 5 years)

Investigators

Sponsor
Beijing Institute of Heart, Lung and Blood Vessel Diseases
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (3)

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