Coronary Artery Disease Clinical Trial
Official title:
Effects of Different Doses of Ticagrelor and Standard-dose Clopidogrel on Platelet Aggregation and Endothelial Function in Diabetic Patients With Stable Coronary Artery Disease
Ticagrelor is an oral, reversibly-binding, direct-acting P2Y12 receptor antagonist used
clinically for the prevention of atherothrombotic events in patients with acute coronary
syndromes (ACS). Guideline recommendations on the use of dual antiplatelet therapy have been
formulated that ticagrelor 90 mg twice daily plus aspirin in preference to clopidogrel 75mg
daily plus aspirin for ACS patients. However, few East Asian patients have been included in
these trials to assess the use of these drugs. In addition, a growing body of data supported
that East Asian might have different adverse event profiles (thrombophilia and bleeding) and
"therapeutic window" compared with white subjects. But it is still not clear whether a low
dose of ticagrelor is superior to clopidogrel in diabetic patients with stable coronary
disease.
Recent studies found that antiplatelet drugs might have anti-inflammatory effects and
protect endothelial function. ACS patients treated by ticagrelor had a significantly higher
increase in levels of circulating progenitor cells compared to those treated by clopidogrel,
suggesting a benefit on endothelial regeneration that may participate in the pleiotropic
property of the drug. This may prompt the regression of blood vessels and the endothelium
stability. But it is not very clear that the effect of low-dose ticagrelor on vascular
endothelial function in diabetic patients with stable coronary artery disease.
Therefore, the investigators performed this randomized, single-blind clinical trial to
observe the effects of different doses of ticagrelor and standard-dose clopidogrel on
platelet aggregation and endothelial function in diabetic patients with stable coronary
artery disease.
| Status | Recruiting |
| Enrollment | 60 |
| Est. completion date | |
| Est. primary completion date | October 2017 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 75 Years |
| Eligibility |
Inclusion Criteria: 1. Stable Coronary Artery Disease (1) stable angina (2) low-risk unstable angina (3) variant angina (4) patients with asymptomatic with appropriate therapy(including percutaneous coronary intervention) 2. Diabetes Exclusion Criteria: 1. ACS 2. planned use of glycoprotein IIb/IIIa receptor inhibitors, adenosine diphosphate (ADP) receptor antagonists, aspirin or anticoagulant therapy during the study period 3. platelet count <100g/L 4. creatinine clearance rate < 30ml/min 5. diagnosed as respiratory or circulatory instability (cardiac shock, severe congestive heart failure NYHA II-IV or left ventricular ejection fraction < 40%) 6. a history of bleeding tendency 7. ticagrelor or clopidogrel allergies |
| Country | Name | City | State |
|---|---|---|---|
| China | Endothelial Function detection by brachial artery ultrasound | Harbin | |
| United States | VerifyNow | San Diego | California |
| Lead Sponsor | Collaborator |
|---|---|
| First Affiliated Hospital of Harbin Medical University |
United States, China,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Inhibition of platelet aggregation | up to 1 month | ||
| Secondary | Endothelial Function | up to 1 month |
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