EUCTR2013-004191-35-BE进行中（未招募）1 期
Evaluation of the effects and plasma concentration of the potent platelet inhibitor ticagrelor, after crushed and non-crushed intake, after semi-urgent coronary bypass and in patients after cardiac arrest. - Ticagrelor-study
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Subject with an acute myocardial infarction with ST elevation
- •Subject with an acute myocardial infarction without ST elevation
- •Subject with unstable angina (progressive angina during past 2 weeks, negative cardiac markers, Trop T < 0,014µg/l
- •First time of taking Brilique
- •= 18 years
- •Possibility to take a blood sample before administration of Brilique
- •Signed Informed Consent, signed by subject or authorized representative, able and willing to provide written informed consent for study participation
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 40
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 60
排除标准
- •Active haemorrhage
- •Moderate or severe liver failure with coagulopathy
- •Pregnancy and lactation
- •A history of an intra cerebral haemorrhage
- •Patient is HIV positive and treated with Ritonavir and /or Atazanavir
- •Patient treated with vitamin K antagonist or with a new oral anti coagulant
- •Hypersensitivity to ticagrelor or any of the exipients
研究者
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