EUCTR2016-003721-41-DK进行中（未招募）1 期
Cangrelor versus Ticagrelor for Early Platelet Inhibition in ST-Elevation Myocardial Infarction. (The CanTi study)
Department of Cardiology, Aarhus University Hospital, Skejby0 个研究点目标入组 80 人开始时间: 2017年11月9日最近更新:
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
- 80
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
入选标准
- •1) Patients triaged for PPCI due to suspicion of STEMI.
- •2) Symptom duration < 12 hours
- •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 30
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 50
排除标准
- •1.Age below 18 years or above 90 years
- •2.Previous inclusion in the study
- •3.Transportation time to PCI-centre < 30 minutes
- •4.Already in treatment with ticagrelor, prasugrel or clopidogrel
- •5.Treatment with oral anticoagulants (warfarin, coumarins, rivaroxaban, apixaban, dabigatran)
- •6.Adjunctive use of glycoprotein IIb/IIIa inhibitor during PCI
- •7.Active bleeding
- •8.Known, severe kidney failure (GFR < 30 ml/min) and/or liver disease
- •9.Women of child bearing ability who are not using contraceptive medication
- •10. Severe mental or psychiatric disease, altered mental state (including unconsciousness) making it impossible to achieve informed consent
研究者
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