此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Impact of Clopidogrel Dose Adjustment According to Platelet Reactivity Monitoring in Patients With High on Treatment Platelet Reactivity Undergoing Percutaneous Coronary Intervention

2012年5月22日 更新者:Assistance Publique Hopitaux De Marseille

Acute coronary syndromes are related to the development of a platelet derived thrombus on a ruptured coronary atheroma. Use of dual antiplatelet therapy aspirin-thienopyridine a significantly reduced the risk of major adverse cardiovascular events (MACE) after percutaneous coronary intervention (PCI). However despite these therapeutic innovations, the rate of MACE in patients treated using PCI and particularly in those suffering of an acute coronary syndrome is around 5% in randomized trials. Within the factors associated with MACE, high on treatment platelet reactivity following clopidogrel loading dose has been identified as a key factor. In fact it is widely recognized that there is a large inter individual variability in clopidogrel responsiveness. In addition several authors have demonstrated a strong link between high on treatment platelet reactivity following clopidogrel loading dose and the occurrence of post PCI MACE. Vasodilator Phosphoprotein index measurement (VASP index) enables a reproducible, standardized and specific assessment of clopidogrel responsiveness.

The investigators previous works have demonstrated that a VASP index ≥ 50% had a high negative predictive value for post PCI MACE in patients undergoing PCI and that tailored clopidogrel loading dose in order to obtain a VASP index < 50% before PCI resulted in a reduction in the rate of post PCI MACE.

Prasugrel is a new generation thienopyridine with a faster and more powerful anti platelet effect compared to clopidogrel. It was shown to be superior to clopidogrel to reduce post PCI MACE in acute coronary syndromes. However in this randomized trial prasugrel achieved an excessive blockade of platelet reactivity responsible for a significant increase in bleeding events in some patients and an insufficient blockade in up to 325% of the remaining patients.

Therefore the investigators hypothesized that a strategy of individually tailored loading and maintenance dose of clopidogrel may be superior to prasugrel standard therapy in achieving an optimal platelet reactivity inhibition in acute coronary syndrome patients undergoing PCI.

研究概览

研究类型

介入性

注册 (实际的)

187

阶段

  • 第三阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Marseille、法国、13354
        • Assistance Publique Hôpitaux de Marseille

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Subject in front of benefited from a coronary angioplasty with setting-up of an endoprothese for a SCA
  • Subject agreeing to be followed over a period of 1 month
  • Subject agreeing to participate in the research and having given its signed enlightened consent

Exclusion Criteria:

  • Subject minor or of more than 75 years old

    • Subject presenting a rate of red blood cells < 4 G/l or a thrombocytopenia > 100 000 / mm3 plaques
    • unaffiliated Subject in a benefit system
    • pregnant or breast-feeding Woman: a pregnancy test will be realized in a systematic way, as well as a stake under contraception of the women old enough to procreate
    • Intolerance or allergy in the aspirin or in the clopidogrel
    • Pathology associated with a life expectancy 6-month-old subordinate according to the investigator
    • haemorrhagic Syndrome threatening the vital forecast, the intra-cranial tumor
    • Contraindication in one of the medicines of the study
    • Severe hepatocellular incapacity
    • Fibrinolyse meadow or hospital intra
    • Ceaseless ventricular arrhythmias
    • State of cardiogenic shock
    • History of cerebral vascular accident
    • Weight lower than 60 kg

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:CLOPIDOGREL GROUP

600 mg clopidogrel will be administered during the first 6 to 12 hours then a measure of platelets reactivity will be done. An additional administration of clopidogrel (600 mg) could be done every 6 hours until to obtain a VASP <50%. No more than 3 * 600mg of clopidogrel will be authorized in this protocol.

Then for patient which have received more than one dose of clopidogrel 600mg , 150 mg per day of clopidogrel will be administrated, for which who have received only one dose of 600mg of clopidogrel , 75 mg per day will be administrated during one month at least.

有源比较器:PRASUGREL GROUP
60 mg the first day then 10 mg per day during one month

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
the biological efficacy of tailored clopidogrel therapy
大体时间:12 months
To compare the biological efficacy of tailored clopidogrel therapy according to the VASP index and prasugrel standard therapy in acute coronary syndromes patients undergoing PCI.
12 months

次要结果测量

结果测量
措施说明
大体时间
clinical efficacy
大体时间:12 MONTHS
Baseline in Systolic Blood Pressure at 6 months
12 MONTHS
Tolerability
大体时间:12 MONTHS
adverse event outcome at 6 months
12 MONTHS

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2011年7月1日

初级完成 (实际的)

2012年5月1日

研究完成 (实际的)

2012年5月1日

研究注册日期

首次提交

2011年8月25日

首先提交符合 QC 标准的

2012年1月6日

首次发布 (估计)

2012年1月9日

研究记录更新

最后更新发布 (估计)

2012年5月23日

上次提交的符合 QC 标准的更新

2012年5月22日

最后验证

2012年5月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅