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A real-world study of anticoagulation in patients with AMI after Primary PCI

A real-world study of anticoagulation in patients with AMI after Primary PCI

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900023824
Enrollment
Unknown
Registered
2019-06-13
Start date
2019-07-01
Completion date
Unknown
Last updated
2020-04-20

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

Conditions

acute myocardial infarction

Interventions

FOND:Use fondaparinux after primary percutaneous coronary intervention
LMWH:Use low molecular weight heparin after primary percutaneous coronary intervention

Sponsors

Shanxi Cardiovascular Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged =18 years, < 85 years; 2. Meets the diagnostic criteria of acute myocardial infarction; 3. PPCI was performed; 4. The patient or legal representative has been informed of the nature of the study, understands the protocol, is able to ensure compliance, and signs the informed consent.

Exclusion criteria

Exclusion criteria: 1. Allergic or contraindicated to anticoagulant and antiplatelet drugs; 2. Cardiac shock, malignant ventricular arrhythmia and mechanical complications were found; 3. CABG was performed; 4. Patients with clear indications of anticoagulation after PPCI; 5. Patients who have long-term anticoagulation indication; 6. Any bleeding tendency, severe blood disease, intracranial parenchymal aneurysms, arteriovenous malformations, suspected aortic dissection, ischemic stroke within the last 6 months, transient ischemic attack or intracranial bleeding history, gastrointestinal and urinary bleeding history within the last 2 weeks; 7. Severe anemia and immune diseases, or (and) hormone therapy; 8. Concurrent diseases such as active infection or cancer ,life expectancy < 12 months; 9. Coagulation dysfunction or moderate or severe insufficiency of liver and kidney function.

Design outcomes

Primary

MeasureTime frame
30d NACE (MACCE and BARC3-5 bleeding);

Countries

China

Contacts

Public ContactJian An

Shanxi Cardiovascular Hospital

18135114037@163.com+86 15803518963

Outcome results

None listed

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