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临床试验/EUCTR2016-000054-35-ES
EUCTR2016-000054-35-ES进行中(未招募)1 期

Effects of Intravenous Lysine Acetylsalicylate versus Oral Aspirin on Platelet Responsiveness in Patients with ST-segment Elevation Myocardial Infarction: a Pharmacodynamic study(ECCLIPSE-STEMI trial) - ECCLIPSE-STEMI trial

Fundación Interhospitalaria Investigación Cardiovascular0 个研究点目标入组 60 人开始时间: 2016年5月17日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
60

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

  • - Age ?18 years
  • - Patient with acute myocardial infarction with ST segment elevation.
  • - Signed informed consent
  • 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 54
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 6

排除标准

  • - Allergy to aspirin, lysine acetylsalicylate , clopidogrel, prasugrel or ticagrelor .
  • - Blood dyscrasias , including a history of thrombocytopenia.
  • - Recent Antiplatelet therapy ( < 14 days) , including aspirin, lysine acetylsalicylate , clopidogrel, prasugrel , ticagrelor , cilostazol , dipyridamole , ticlopidine or glycoprotein IIb / IIIa .
  • - Chronic treatment with oral anticoagulants.
  • - Active bleeding .
  • - Recent history of stroke, transient ischemic attack or intracranial hemorrhage ( < 6 months prior to inclusion period ) .
  • - Severe renal impairment , defined as glomerular filtration rate ( Cockroft -Gault formula ) < 30 mL / min .
  • - Elevated transaminase > 2.5 times the normal limit .
  • - Active Neoplasia .
  • - Pregnancy and lactation.
  • - Concomitant terminal disease .
  • - Inclusion in another clinical trial .

研究者

发起方
Fundación Interhospitalaria Investigación Cardiovascular

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