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临床试验/ISRCTN11629138
ISRCTN11629138已完成不适用

European Pharmacogenetics of Anticoagulant Therapy

niversity of Liverpool (UK)0 个研究点目标入组 706 人开始时间: 2010年10月29日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
706

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

入选标准

  • 1. Patients with either venous thromboembolism (VTE) or atrial fibrillation (AF) requiring coumarin therapy for at least 12 weeks and a target International Normalised Ratio (INR) in the low intensity range (INR range 2 - 3)
  • 2. Aged greater than or equal to 18 years, either sex
  • 3. Ability to attend scheduled visits
  • 4. Signed informed consent

排除标准

  • 1. Presence of a mechanical heart valve
  • 2. Severe cognitive impairment which affects adherence to therapy as judged by the responsible physician
  • 3. Known genotype CYP2C9 or VKORC1 at start of the study
  • 4. Previous or current treatment with any coumarin (maximum one dose allowed)
  • 5. Pregnancy or lactation
  • 6. Non-eligible subject according to the treating physician
  • 7. A blood transfusion within the last two weeks or bone marrow transplantation at any time

研究者

发起方
niversity of Liverpool (UK)

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European Pharmacogenetics of Anticoagulant Therapy | 临床试验