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临床试验/NCT00360386
NCT00360386已完成2 期

Assessment of the Best Loading Dose of Clopidogrel to Blunt Platelet Activation, Inflammation and Ongoing Necrosis.

Sanofi0 个研究点目标入组 110 人开始时间: 2004年3月1日最近更新:
适应症
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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

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

发起方
Sanofi
申办方类型
Industry

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