Prospective Coronary Heart Disease Cohort
A Prospective Longitudinal Multi-Omics Cohort of Patients With Coronary Heart Disease Undergoing Coronary Angiography
1 other identifier
observational
50,000
1 country
1
Brief Summary
To evaluate the biomarkers for the prognosis of coronary heart disease, patients with coronary heart disease will be recruited and followed up for at least 2 years.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2022
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 21, 2022
CompletedFirst Submitted
Initial submission to the registry
January 9, 2023
CompletedFirst Posted
Study publicly available on registry
January 26, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 21, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 21, 2027
February 13, 2023
February 1, 2023
5 years
January 9, 2023
February 9, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
major adverse cardiovascular events
all-cause mortality, cardiovascular mortality, ischemic stroke, heart failure and rehospitalization
2-year outcome and long-term outcome
Eligibility Criteria
Patients with coronary heart diseases undergoing coronary angiography and healthy control subjects undergoing routine physical examination in physical examination department.
You may qualify if:
- Diagnosed as coronary heart disease or with unexplained chest pain needed to undergo coronary angiography.
- Healthy subjects undergoing routine physical examination in the physical examination department and willing to sign informed consent will be recruited as control subjects.
You may not qualify if:
- With malignant tumors, infectious diseases and advanced liver diseases.
- Won't sign an inform consent.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Shandong First Medical Universitylead
- Jinan Central Hospitalcollaborator
- Shandong Provincial Hospitalcollaborator
- The Second Affiliated Hospital of Shandong First Medical Universitycollaborator
- Qianfoshan Hospitalcollaborator
Study Sites (1)
Shandong First Medical University
Jinan, Shandong, 277500, China
Biospecimen
blood and fecal samples
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Tao Xu, Dr.
Shandong First Medical University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 9, 2023
First Posted
January 26, 2023
Study Start
January 21, 2022
Primary Completion (Estimated)
January 21, 2027
Study Completion (Estimated)
January 21, 2027
Last Updated
February 13, 2023
Record last verified: 2023-02
Data Sharing
- IPD Sharing
- Will not share