Overview

Low-dose of Ticagrelor and Standard-dose Clopidogrel on Platelet Effects in Chinese Patients With Stable CAD.

Status:
Unknown status
Trial end date:
2019-08-29
Target enrollment:
0
Participant gender:
All
Summary
Ticagrelor has been demonstrated to provide a more rapid and more powerful inhibition of platelet aggregation compared with clopidogrel in coronary artery disease (CAD) patients. However, current guidelines recommend ticagrelor 90 mg twice daily might not be suitable for patients of Chinese. Therefore, the investigators performed this study to observe the efficacy of 60-mg ticagrelor in comparison to 75-mg clopidogrel in Chinese patients with stable CAD.
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
First Affiliated Hospital of Harbin Medical University
Treatments:
Clopidogrel
Ticagrelor
Ticlopidine
Criteria
Inclusion Criteria:

- Patients were eligible to participate if they were aged ≥18 years and ≤ 75 Years

- Subjects had documented stable CAD (defned as stable angina pectoris and objective
evidence of CAD, a previous MI, or previous revascularization with percutaneous
coronary intervention or coronary artery bypass grafting)

- Women were required to be postmenopausal or surgically sterile

- Patients who were taking clopidogrel or ticagrelor were required to discontinue these
agents at least 14 days before randomization

Exclusion Criteria:

- Acute coronary syndrome (ACS)

- planned use of glycoprotein IIb/IIIa receptor inhibitors, adenosine diphosphate (ADP)
receptor antagonists other than the study medication, or anticoagulant therapy during
the study period

- platelet count <10*10^4/ul

- creatinine clearance rate < 30ml/min

- diagnosed as respiratory or circulatory instability (cardiac shock, severe congestive
heart failure NYHA II-IV or left ventricular ejection fraction < 40%)

- a history of bleeding tendency

- allergy to aspirin, ticagrelor or clopidogrel

- diabetes patients