NCT00360386已完成2 期
Assessment of the Best Loading Dose of Clopidogrel to Blunt Platelet Activation, Inflammation and Ongoing Necrosis.
适应症
相关药物
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- Sanofi
- 入组人数
- 110
- 主要终点
- Maximum intensity of platelet aggregation induced by ADP 5 µmol/L.
研究概览
简要总结
- To compare the Kinetics of inhibition of platelet aggregation (aggregometry) and platelet activation (flow cytometry) with different loading doses of clopidogrel
- To evaluate the effect on various parameters of inflammation and necrosis and the safety of these loading doses
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 85 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patient hospitalised with ischemic symptoms (onset < 48 hours) and at least one of the following characteristics of NSTEMI:
- •ECG ST or T changes
- •positive troponin
- •Patient treated on admission with 250-500 mg aspirin (oral or IV) and who will receive low dose aspirin (< or = 100 mg daily) from the next day on
- •Patient treated with bid LMWH (indicated dosage for this indication)
排除标准
- •Catheterization scheduled within 24 hours after randomisation
- •Patient presenting an absolute contra-indication to the use of clopidogrel and/or ASA:
- •- history of drug allergy to thienopyridine derivatives or ASA
- •Severe uncontrolled hypertension (BP > 180 / 100 despite therapy)
- •Platelet count < 100 000 / mm3
- •Neutrophil count < 1800 / mm3
- •Patient with increased risk of bleeding, such as severe hepatic insufficiency, current peptic ulceration, proliferative diabetic retinopathy
- •History of severe systemic bleeding
- •Patient with any contraindication to LMWH
- •Patient treated with clopidogrel within the last 10 days
- •Patient treated with oral anticoagulants or hirudin or planned to receive these products during the hospitalisation period
- •Patient treated with ticlopidine, dipyridamol, NSAIDs (including Cox1 and Cox2 inhibitors), cilostazol, GPIIb IIIa antagonists or planned to receive any of these products within the next 24 hours following randomisation.
- •Patient whose arm venous status is incompatible with an indwelling catheter
- •Patient presenting an evolving cancer
- •Patient with NYHA class IV heart failure
- •Intubated and ventilated patient
结局指标
主要结局
Maximum intensity of platelet aggregation induced by ADP 5 µmol/L.
次要结局
- Kinetic profile by aggregometry. Kinetic profile of platelet activation by flow cytometry - Inflammation parameters/markers of necrosis. Death, myocardial infarction, ischemic recurrences leading to revascularisation and/or rehospitalisation.Safety.
研究者
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