跳至主要内容
临床试验/EUCTR2012-003897-21-IT
EUCTR2012-003897-21-IT进行中(未招募)不适用

Effects of TIcaGREloR on Circulating Microparticles and Micro-RNAs in patients with Non ST Elevation Acute Coronary Syndromes - TIGER-M study

POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI0 个研究点开始时间: 2012年12月28日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

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

  • -PATIENT WITH NON-ST ELEVATION ACUTE CORONARY SYNDROMES - men aged between 50 and 80 years - postmenopausal women
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 24
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 40

排除标准

  • men aged <50 years or >80 years - impossibility to give informed consent - women of childbearing age - diabetes mellitus - severe renal failure (CrCl < 30 ml/min) - infective, neoplastic or autoimmune diseases - ACS and /or TIA/stroke in the previous three months - trauma or surgical operations in the previous three months - active hemorrhage - fibrinolytic therapy within 24 hours before randomization, - a need for oral anticoagulation therapy - an increased risk of bradycardia - drugs study hypersensitivity (including aspirin) - moderate to severe hepatic impairment 15 - co-administration of ticagrelor or clopidogrel with strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin, nefazodone, ritonavir, and atazanavir)
  • GRACE RISK SCORE >140
  • In stent restenosis

研究者

发起方
POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI

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