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临床试验/CTIS2024-512436-29-00
CTIS2024-512436-29-00进行中(未招募)1 期

VerifyNow to Optimise Platelet Inhibition in Coronary Acute Syndrome (VERONICA) - EPIC17

Fundacion Epic0 个研究点目标入组 634 人开始时间: 2024年3月17日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
634

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 65+(—)
性别
All

入选标准

  • Patients with age 18 years or above; Patient is able to understand the nature of study and has provided written informed consent; Patients with Acute Coronary Syndrome and who underwent PCI during the admission with absorbable polymer stent who have been discharged on double antiplatelet therapy with Acetylsalicylic Acid and Ticagrelor or Prasugrel

排除标准

  • Patients with history of intracranial bleeding; Patients with contraindication for the use of Acetylsalicylic Acid or Clopidogrel or Ticagrelor or Prasugrel; Patients with major ischemic or hemorrhagic events during the first month; Patients with Thrombocytopenia <50,000 /µL; Patients with permanent oral anticoagulation; Patient is pregnant or breast feeding;Patients with impossibility to complete 1 year of follow-up; Patient´s life-expectancy is less than 24 months

研究者

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