跳至主要内容
临床试验/EUCTR2011-006210-13-IT
EUCTR2011-006210-13-IT进行中(未招募)不适用

Prospective randomized ARMYDA 600x2 STUDY - ARMYDA600X2

IVERSITA' CAMPUS BIOMEDICO0 个研究点目标入组 300 人开始时间: 2012年3月7日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
300

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

  • ? Patients with stable angina and inducible myocardial ischemia who are candidates for elective percutaneous angioplasty.
  • 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 100
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 200

排除标准

  • ? Patients with acute coronary syndromes. ? Patients candidates to receive oral anticoagulant therapy. ? Patients with thrombocytopenia (platelets <70.000/mm3). ? Patients who underwent a coronary artery bypass graft in the previous three months. ? Severe left ventricular dysfunction with left ventricular ejection fraction <30%. ? Renal failure with creatinine> 2 mg / dl based. ? Patients with a recent episode of major bleeding (<6 months)

研究者

发起方
IVERSITA' CAMPUS BIOMEDICO

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