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临床试验/NL-OMON32667
NL-OMON32667招募中4 期

Coronary versus Intravenous abCiximab administration during Emergency Reperfusion Of ST-segment elevation myocardial infarction - the CICERO trial - CICERO

niversitair Medisch Centrum Groningen0 个研究点目标入组 530 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
入组人数
530

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • - a diagnosis of STEMI defined by
  • a. chest pain suggestive for myocardial ischemia for at least 30 minutes before hospital admission
  • b. time from onset of symptoms of less than 12 hours
  • c. ECG with ST-segment deviation of more than 0.1 mV in 2 or more leads
  • - primary PCI performed
  • - verbal followed by written informed consent

排除标准

  • -rescue PCI after thrombolytic therapy
  • -need for emergency coronary artery bypass grafting
  • -presence of cardiogenic shock
  • -known existence of a life-threatening disease with a life expectancy of less than 6 months
  • -inability to provide informed consent
  • -age below 18 years
  • -Contra-indications for the use of abciximab (active internal bleeding, history of stroke within 2 years, recent major surgery or intracranial or intraspinal trauma or surgery within 2 months, intracranial neoplasm, arteriovenous malformation or aneurysm, bleeding diathesis, severe uncontrolled hypertension, thrombocytopenia, vasculitis, hypertensie or diabetic retinopathy, severe liver or kidney failure, and hypersensitivity to murine proteins).

研究者

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