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临床试验/NL-OMON51290
NL-OMON51290招募中3 期

Multicentre prospective trial for extracranial malignant germ cell tumours including a randomized comparison of Carboplatin and Cisplatin - MAKEI-V

Rheinische Friedrich-Wilhelms Universität Bonn0 个研究点目标入组 25 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
25

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

年龄范围
0 至 64(—)

入选标准

  • - Confirmed extracranial MGCT up to 17 11/12 years of age or patients with
  • ovarian primaries up to 29 11/12 years of age on the date of written informed
  • - Diagnosis of a chemotherapy-naïve extracranial MGCT
  • - Written informed consent of patients and/or their parents according to
  • national law prior to trial entry
  • - Karnofsky-Index of >70% or ECOG-Status 0-II
  • - Negative pregnancy test within 7 days prior to starting treatment for female
  • patients of childbearing potential, in case of ß-HCG secreting MGCT pregnancy
  • has to be excluded by appropriate methods

排除标准

  • - Pregnancy
  • - Lactation
  • - Incomplete data at trial entry preventing risk group allocation
  • - HIV-positivity
  • - Live vaccine immunization within two weeks before start of protocol treatment
  • - Sexually active adolescents not willing to use highly effective contraceptive
  • method (pearl index <1)
  • until 12 months after end of chemotherapy
  • - Current or recent (within 30 days prior to date of informed written consent)
  • treatment with another investigational drug or participation in another
  • interventional clinical trial, except trials with different end points than
  • MAKEI V that can run in parallel to MAKEI V without influencing that trial
  • - Any other medical, psychiatric or drug related condition, or social condition
  • incompatible with protocol treatment.

研究者

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