跳至主要内容
临床试验/EUCTR2008-004991-28-DE
EUCTR2008-004991-28-DE进行中(未招募)不适用

Assessment of focal liver lesions in fluoroscopic MR using Primovist and fast dynamic imaging sequences for interventional purposes - Liver lesions in fluoroscopic MR

Medical Faculty Magdeburg0 个研究点目标入组 34 人开始时间: 2009年2月27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
入组人数
34

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

  • 1.age: between 18 and 85 years
  • 2.patients with focal liver lesions between 0.5 and 5 cm (reported in previous CT or MR investigations) who are scheduled for biopsy for clinical reasons.
  • 3.if female, postmenopausal or surgically sterilized
  • 4.willing and able to undergo all study procedures
  • 5.having voluntarily provided written and fully informed consent
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1.coagulation disorder (TPZ < 70%, PTT > 35 sec. , platelets < 100000/ml)
  • 2.history of severe allergic reaction to MR contrast media or to Primovist (or on of its ingredients)
  • 3.severe and moderate renal failure (GFR <60 mL as calculated according to the MDRD or Cockroft-Gault formula)
  • 4.women who are pregnant, lactating or who are of childbearing potential
  • 5.patients being clinically unstable
  • 6.uncooperative, in the investigator’s opinion
  • 7.any contraindication to MR examinations
  • 8.having been previously enrolled in this study
  • 9.participating in another clinical trial

研究者

发起方
Medical Faculty Magdeburg

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