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临床试验/EUCTR2015-005046-55-SE
EUCTR2015-005046-55-SE进行中(未招募)1 期

Evaluation of [68Ga]PSMA PET/MRI in intermediate and high risk prostate cancer – a comparison with mpMRI, [11C]ACE PET/CT and histopathological validation

meå University Hospital0 个研究点开始时间: 2016年6月9日最近更新:

试验速览

阶段
1 期
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
Male

入选标准

  • -Histologically confirmed intermediate/high risk prostate cancer
  • - =2 months since last biopsy of the prostate
  • - Gleason 3+4 or higher
  • -Written informed consent
  • -> 18 years
  • 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 15
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 40

排除标准

  • -Non MR-safe implants or other contraindication to MRI,PET or CT
  • -WHO PS>1
  • -TUR-P within 6 months
  • -Metastatic disease in skeleton, parenchymal organs or lymph nodes outside the pelvis
  • -Creatinine clearance < 30ml/min (acc. to http://www.fass.se/LIF/produktfakta-/kreatinin.jsp)

研究者

发起方
meå University Hospital

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Evaluation of [68Ga]PSMA PET/MRI in intermediate and... | 临床试验