Causation And Prognosis Analyses of Coronary Artery Diseases: A Longitudinal Cohort Study
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Coronary Artery Disease. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Causation And Prognosis Analyses of Coronary Artery dIseases: a longiTudinal Cohort studY
Overview
This study is a single-center, historical prospective cohort study including patients diagnosed with coronary artery diseases, including stable angina pectoris, unstable angina pectoris, non-ST-segment elevation myocardial infarction, ST-segment elevation myocardial infarction, latent coronary artery diseases and ischemic cardiomyopathy. The primary outcome of the study is all-cause and cardiovascular mortality. We aim to investigate associations of established or suspected cardiovascular risk factors and the outcome in population with coronary artery dieseases in this real-world cohort.
Primary outcome measures
- All-cause mortality [Time frame: Through study completion, an average of 5 years]
- Cardiovascular mortality [Time frame: Through study completion, an average of 5 years]]
Eligibility criteria
Inclusion criteria
- Patients over 18 years old;
- Patients with clinical diagnosis of coronary artery diseases, including stable angina pectoris, unstable angina pectoris, non-ST-segment elevation myocardial infarction, ST-segment elevation myocardial infarction, latent coronary artery diseases and ischemic cardiomyopathy.
Exclusion criteria
- Patients unable to provide informed consent.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
China · 1 center
- The First Affiliated Hospital, Sun Yat-sen Univerity — Guangzhou
Identifiers
NCT: NCT07480512 · CAPACITY