the Efficacy and Safety of Indobufen and Low-dose Aspirin in Different Regimens of Antiplatelet Therapy
Coronary Atherosclerosis

About this trial
This is an interventional treatment trial for Coronary Atherosclerosis focused on measuring Light Transmittance Aggregometry, Indobufen, Aspirin, Plasma Thromboxane, Urine 11-dehydro thromboxane
Eligibility Criteria
Inclusion Criteria:
Clinical diagnosis of coronary atherosclerosis without indications for stent implantation .
Patient aged >18 years and ≤75years. Must be able to swallow tablets
Exclusion Criteria:
Aspirin resistance; uncontrolled hypertension (> 160 / 100mmHg); hemoglobin <100g / L; hemorrhagic disease or bleeding tendency history; taking other non-steroidal drugs; severe liver disease history; malignant neoplasms; active gastric mucosa bleeding; PCI history; coronary artery bypass surgery; cardiac function grade Ⅳ.
Sites / Locations
- First Affiliated Hospital of Nanjing Medical University
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm 6
Arm 7
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
aspirin 100mg/d therapy
aspirin 100mg/2d therapy
aspirin 100mg/3d therapy
aspirin 50mg bid therapy
aspirin 75mg/d therapy
aspirin 50mg/d therapy
indobufen 100mg bid therapy
Group1: aspirin 100 mg/d;
Group2: aspirin ;
Groups3: aspirin ;
Groups4: morning 50mg evening 50mg;
Group5: aspirin 75mg / d;
Group6: aspirin 50mg / d;
Group7: 100mg bid