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RECRUITINGOBSERVATIONAL

Prognosis Prediction System of Patients With Cardiovascular and Cerebrovascular Diseases Based on Multi-omics

Prognosis Prediction System of Patients With Cardiovascular and Cerebrovascular Diseases Based on Multi-omics (PROSPECT): a National, Multicenter, Retrospective-prospective, Cohort Study

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The etiology and specific pathogenesis of many cardiovascular diseases such as coronary atherosclerosis, cardiomyopathy, atrial fibrillation, and stroke are still unclear. Improving diagnosis and treatment, clarifying the pathogenesis, and providing scientific basis for the prevention and treatment are hot research topics in the study of cardiovascular and cerebrovascular diseases. This study intends to collect clinical data and biological specimen data of patients with cardiovascular and cerebrovascular diseases who meet the inclusion and exclusion criteria, and use multi-omics technology to deeply understand the pathogenic mechanisms of cardiovascular and cerebrovascular diseases and provide new ideas for specific and individualized treatment of patients with cardiovascular and cerebrovascular diseases, to construct early predictive prognostic models and provide a basis for effective treatment of clinical practice in patients with cardiovascular and cerebrovascular diseases.

Who May Be Eligible (Plain English)

Who May Qualify: - Patients who are regularly visited and followed up in the appropriate patient; department. - All patients met at least one of the following diagnostic criteria for cardiovascular and cerebrovascular diseases: - coronary artery disease group; - arrhythmia group; - heart valve disease group; - aortic dissection group; - cardiac masses group; - myocarditis group; - hypertension group; - cardiomyopathy group; - structural heart disease group; - ischemic cerebrovascular disease group; - hemorrhagic cerebrovascular disease group; - intracranial space occupying lesion group. Who Should NOT Join This Trial: - Age \<3 years or \>80 years old; - Pregnant and lactating women; - The patient declined to provide willing to sign a consent form to participate in the study; - None of the above was met, but the patient was temporarily unable to sign the willing to sign a consent form form due to coma and other reasons, and no legal representative signed it instead. Depending on the patient's condition, the patient may not be able to regain consciousness and sign the willing to sign a consent form form. Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Patients who are regularly visited and followed up in the appropriate patient; department. * All patients met at least one of the following diagnostic criteria for cardiovascular and cerebrovascular diseases: * coronary artery disease group; * arrhythmia group; * heart valve disease group; * aortic dissection group; * cardiac masses group; * myocarditis group; * hypertension group; * cardiomyopathy group; * structural heart disease group; * ischemic cerebrovascular disease group; * hemorrhagic cerebrovascular disease group; * intracranial space occupying lesion group. Exclusion Criteria: * Age \<3 years or \>80 years old; * Pregnant and lactating women; * The patient declined to provide informed consent to participate in the study; * None of the above was met, but the patient was temporarily unable to sign the informed consent form due to coma and other reasons, and no legal representative signed it instead. Depending on the patient's condition, the patient may not be able to regain consciousness and sign the informed consent form.

Treatments Being Tested

OTHER

Observational; No Interventions were given.

Observational; No Interventions were given.

Locations (1)

First Affiliated Hospital of Xian Jiantong University
Xi'an, Shaanxi, China