Last updated: December 20, 2021
Sponsor: First Affiliated Hospital of Harbin Medical University
Overall Status: Completed
Phase
4
Condition
Coronary Artery Disease
Thrombosis
Vascular Diseases
Treatment
N/AClinical Study ID
NCT04001894
20190515
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:•
- Aged ≥18 years
- Subjects had documented with stable CAD
- Women were required to be postmenopausal or surgically sterile
- Patients were required to discontinue clopidogrel or ticagrelor at least 14 daysbefore randomization
- Patients were required to discontinue aspirin at least 14 days before randomization.
Exclusion
Exclusion Criteria:
- Acute coronary syndrome
- Planned use of glycoprotein IIb/IIIa receptor inhibitors, adenosine diphosphate (ADP)receptor antagonists other than the study medication, or anticoagulant therapy duringthe study period
- Platelet count <10×10^4/μL
- Hstory of bleeding tendency
- Diagnosed as respiratory or circulatory instability
- Allergy to ticagrelor or clopidogrel
Study Design
Total Participants: 50
Study Start date:
July 02, 2019
Estimated Completion Date:
December 09, 2020
Study Description
Connect with a study center
Thrombelastogram
Harbin, Heilongjiang 150001
ChinaSite Not Available

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