The aim of the current study is to compare the antiplatelet efficacy and safety of
clopidogrel napadisilate and clopidogrel bisulfate in Coronary Artery Disease (CAD) patients
after coronary stent implantation.
Drug: clopidogrel napadisilate + aspirin
Drug: clopidogrel bisulfate + aspirin
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Full eligibility criteria for NCT01584791
Ages eligible for Study
20 Years to 85 Years
Genders eligible for Study
Accepts Healthy Volunteers
Korean men and women between the age of 20 and 85
Patients who were diagnosed as having CAD
Patients who were planned to undergo PCI
Patients who were not treated with PCI or intended to treat with PCI but failed
Patients who were were taking or had taken other antiplatelet or anticoagulant for more than 2 weeks within the prior 30 days
Patients who were had a history of alcohol abuse or intoxication; (4) had hypersensitivity to clopidogrel or aspirin
Patients who were had hypersensitivity to clopidogrel or aspirin
Patients who were had abnormal laboratory results indicative of liver disease
Patients who were had blood coagulation disorders, uncontrolled severe hypertension, active bleeding, or history of severe bleeding, such as intracranial hemorrhage or ulcer bleeding
Patients who were were pregnant, breastfeeding, or not using effective methods of contraception
Patients who were had other contraindication to study drug
Patients who were had participated in another clinical study within 4 weeks prior to the start of this study
All locations for NCT01584791
Korea, Republic of (1)
Seoul National University
Seoul, Korea, Republic of, 110-744
View full eligibility
Tris trial is registered with FDA with number: NCT01584791. The sponsor of the trial is Seoul National University Hospital and it is looking for 148 volunteers for the current phase.
Official trial title:
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