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临床试验/NL-OMON39774
NL-OMON39774已完成不适用

Prostate Cancer Molecular Medicine - PCMM

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 496 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
496

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • planned to undergo prostate biopsies according to standard practice
  • signed informed consent;Group 2:
  • cT1-3Nx-0Mx-0 prostate cancer
  • scheduled for radical prostatectomy according to standard practice
  • signed informed consent

排除标准

  • Group 2 only:
  • known allergy to contrast agents or sulphur hexafluoride micro bubbles
  • documented acute prostatitis or urinary tract infections within 8 weeks prior to inclusion
  • severe cardiac condition
  • any clinically unstable cardiac condition within 7 days prior to contrast agent administration such
  • - evolving or ongoing myocardial infarction
  • - typical angina at rest
  • - significant worsening of cardiac symptoms
  • - recent coronary artery intervention or other factors suggesting clinical instability (e.g., recent
  • deterioration of ECG, laboratory or clinical findings)
  • - acute cardiac failure, class III/IV cardiac failure
  • - severe cardiac rhythm disorders
  • - right-to-left shunts
  • known severe pulmonary hypertension (pulmonary artery pressure >90 mmHg) or uncontrolled
  • systemic hypertension or respiratory distress syndrome
  • renal insufficiency (GFR < 30 ml/min)
  • vulnerable for epilepsy
  • presence of a pacemaker or other implants or clamps

研究者

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