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Comparison the efficacy and safety of ticagrelor and TEG-optimized clopidogrel on emergency PCI for patients with acute non-ST segment-elevation myocardial infarction

Comparison the efficacy and safety of ticagrelor and TEG-optimized clopidogrel on emergency PCI for patients with acute non-ST segment-elevation myocardial infarction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800014908
Enrollment
Unknown
Registered
2018-02-17
Start date
2018-04-02
Completion date
Unknown
Last updated
2018-02-19

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

Conditions

acute non-ST-elevation myocardial infarction

Interventions

ticagrelor group:180mg loading dose of ticagrelor, followed by 90mg q12h.
TEG-optimizaed clopidogrel group: 600mg loading dose of clopidogrel, with TEG-guided upstream tirofiban, followed by clopidogrel 75mg/day
intensive statin group:Rosuvastatin of 20mg are given twice in the first 24 hours, followed by 20mg/day
low-dose statin group:Rosuvastatin are given 5mg/day

Sponsors

Tianjin Cardiogy Institue
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged between from 18 to 75 years; 2. diagnosed of acute NSTEMI; 3. early PCI within 24 hours is planning according to China PCI guideline in 2016; 4. Severe stenostic or thrombotic lesions in epicardial coronary arteries.

Exclusion criteria

Exclusion criteria: 1. Urgency PCI with 2 hours is indicated, including hemodynamic compromise or cardiogenic shock; refractory angina; malignant arrhythmia; mechanical complications; acute heart failure; transient ST segment elevation; 2. P2Y12 receptor antagonists and/or intensive statin have been used within the 30 days before; 3. Indicators of anticoagulants; 4. Hepatic and renal dysfunction (serum creatinine>221umol/L, AST/ALT above the 5 times of upper limit, or history of cirrosis); 5. Complications of severe infection or malignant neoplasm; 6. Active digestive ulcer, anemia, coagulant dysfunction, or hypersensitive to drugs in this trial; 7. Hematopoitic system disease; 8. History of ischemic or hemorrhagic stroke.

Design outcomes

Primary

MeasureTime frame
cardiovasular mortality;stent thrombosis;recurrent myocardial infarction;urgent revascularization;ischemic stroke;

Secondary

MeasureTime frame
CK-MB;serum soluble CD40L;MA-ADP;

Countries

China

Contacts

Public ContactJingjin Che

the Second Hospital of Tianjin Medical Unniversity

jingjinche@aliyun.com+86 18630918358

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 23, 2026