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Prognostic factors associated with coronary heart disease: a multicenter, prospective study

Prognostic factors associated with coronary heart disease: a multicenter, prospective study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024580
Enrollment
Unknown
Registered
2019-07-18
Start date
2019-11-01
Completion date
Unknown
Last updated
2019-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

coronary heart disease

Interventions

Case series:Nil

Sponsors

The First affiliated hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged at least 18 years to 80 years; 2. Coronary angiography confirmed at least one coronary artery stenosis> 50%; 3. At least one clinical phenotype of coronary heart disease: stable angina or acute coronary syndrome.

Exclusion criteria

Exclusion criteria: 1. combined with severe valvular heart disease; 2. combined with severe congenital heart disease; 3. Combined hyperthyroidism, anemia and other high-powered heart disease; 4. with pulmonary heart disease; 5. with hypertrophic obstructive cardiomyopathy; 6. Severe hypotension (SBP 160 mmHg before PCI, and / or DBP> 100 mmHg); 8. Liver dysfunction (defined as ALT or total bilirubin is greater than the normal upper limit of 3 times); 9. Renal insufficiency (defined as serum creatinine greater than 1.5 times the normal upper limit); 10. High-risk bleeding patients, such as thrombocytopenia, blood diseases and other diseases; 11. active peptic ulcer and skin ulcers; 12. A patient who is allergic to clopidogrel, tegrellol, or aspirin; 13. Patients with a history of cardiogenic shock within two weeks; 14. pregnant and lactating women, during treatment can not be strict contraception of women of childbearing age; 15. In the past 3 months participated in other clinical researchers; 16. Persons who do not have legal or legal competence; 17. Any condition that the investigator considers unsuitable for participation in the clinical study.

Design outcomes

Primary

MeasureTime frame
all-cause mortality;Cardiac mortality;stroke;BARC2 or more bleeding events;readmission;Target vessel revascularization;Recurrent myocardial infarction;Stent thrombosis;Heart Failure;

Countries

China

Contacts

Public ContactJinying Zhang

The First Affiliated Hospital of Zhengzhou University

jyzhang@zzu.edu.cn+86 13503830283

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026