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临床试验/NCT02038309
NCT02038309已完成不适用

Persistent Platelet Reactivity in Acute Coronary Syndrome

Hopital Lariboisière1 个研究点 分布在 1 个国家目标入组 106 人开始时间: 2013年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
106
试验地点
1
主要终点
maximum aggregation intensity

研究概览

简要总结

Study of persistent platelet reactivity during acute coronary syndrome. Patients are included at admission to the hospital. Platelet aggregation is evaluated by platelet function testing after blood sampling during hospitalization. No changes in treatment is planned.

详细描述

Blood samples are performed on day 2 and 4 and collected with usual blood samples and analyzed by the laboratory. Maximal aggregation intensity and velocity are measured by light transmission aggregometry induced by arachidonic acid (AA) or adenosine diphosphate (ADP). Platelet function analyzer will be also used. No changes in treatment in response to the results is planned.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • acute coronary syndrome with elevation in troponin

排除标准

  • anticoagulant treatment

结局指标

主要结局

maximum aggregation intensity

时间窗: day 2

Light transmission aggregometry following exposition to arachidonic acid 0.5mg/ml during the acute phase (day2-day 5)

次要结局

  • Maximum aggregation intensity(Chronic phase (day 30 to day 60))

研究者

发起方
Hopital Lariboisière
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr Jean-Guillaume DILLINGER

Department of Cardiology

Hopital Lariboisière

研究点 (1)

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