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Study on the pathogenesis, diagnosis and prognosis of coronary heart disease by microbiology and metabonomics

Study on the pathogenesis, diagnosis and prognosis of coronary heart disease by microbiology and metabonomics

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900027476
Enrollment
Unknown
Registered
2019-11-15
Start date
2019-11-20
Completion date
Unknown
Last updated
2019-11-18

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

Conditions

Coronary heart disease

Interventions

ACS group vs. Stable CAD group:N/A

Sponsors

The First Affiliated Hospital of Xinjiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-80 years; 2. Coronary angiography confirmed at least one coronary artery stenosis >50%. 3. or at least one troponin increase or decrease value > 99% of the upper limit of the reference value, accompanied by at least one of the following: (1) Symptoms of ischemia; (2) New ST segment and T wave changes or ECG showing new left bundle branch block; (3) ECG shows pathological Q wave progression; (4) Imaging evidence shows reduced myocardial contraction or abnormal local wall contraction. 4. Or a dose-loaded dual antiplatelet drug (ASA 300mg + clopidogrel 300mg) has been given before PCI.

Exclusion criteria

Exclusion criteria: 1. Combined with severe heart valve disease. 2. Combined with severe congenital heart disease. 3. Combined with hyperdynamic heart disease such as hyperthyroidism and anemia. 4. Combined with pulmonary heart disease. 5. Combined with hypertrophic obstructive cardiomyopathy. 6. Severe hypotension (SBP 160 mm Hg, and / or DBP > 100 mm Hg). 8. Hepatic insufficiency (defined as ALT or total bilirubin greater than 3 times the upper limit of normal). 9. Renal dysfunction (defined as serum creatinine greater than 1.5 times the upper limit of normal). 10. Patients at high risk of bleeding, such as thrombocytopenia, blood system diseases, etc. 11. Active peptic ulcer and skin ulcers. 12. Patients who are allergic to clopidogrel, ticagrelor, and aspirin. 13. Patients with a history of cardiogenic shock within two weeks. 14. Pregnant and lactating women, women of childbearing age who are not strictly contraceptive during treatment. 15. Those who do not have legal capacity or limited legal capacity.

Design outcomes

Primary

MeasureTime frame
all-cause mortality (ACM) and cardiac mortality (CM);

Secondary

MeasureTime frame
Stroke, BARC level 2 or higher bleeding events, rehospitalization, and major cardiac adverse events (MACE) included all-cause death, stent thrombosis, cardiac death, target vessel revascularization, and stent thrombosis.;

Countries

China

Contacts

Public ContactXiang Xie

The First Affiliated Hospital of Xinjiang Medical University

xiangxie999@sina.com+86 15099169036

Outcome results

None listed

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