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临床试验/NL-OMON51513
NL-OMON51513招募中不适用

International multicenter observational study to determine the diagnostic sensitivity of plasma metanephrines and urinary catecholamines and metabolites compared to standard evaluation procedures in children with high risk neuroblastoma - Metanephrines

Centre Hospitalier Universitaire Vaudois-CHUV0 个研究点目标入组 30 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
招募中
入组人数
30

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
0 至 17(—)

入选标准

  • Patients with confirmed high risk neuroblastoma (clinical and/or biological)
  • Patients treated within or according to SIOPEN HR-NBL-2 clinical trial
  • Age < 18 years at inclusion, male or female
  • Ethic committee approval for each participating site
  • Informed consent signed by the legal representatives and/or by the child
  • according to local regulations

排除标准

  • Renal insufficiency (creatinine clearance according to Schwartz formula <
  • 60ml/min/m2)
  • Absence of histological confirmation of high risk neuroblastoma
  • Lack of consent

研究者

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