跳至主要内容
临床试验/NL-OMON47606
NL-OMON47606已完成不适用

Medical assessment of adverse health outcomes in Dutch childhood cancer survivors; a nationwide project (DCOG LATER study) DCOG LATER substudy: Sexual function and psychosexual development in long-term childhood cancer survivors - DCOG LATER - sexual function and psychosexual development

Stichting Kinderoncologie Nederland0 个研究点目标入组 6,500 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
发起方
入组人数
6,500

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

  • The general study design involves a nation-wide multicentre retrospective
  • cohort study including the entire DCOG-LATER cohort of CCS according to the
  • DCOG-LATER inclusion criteria:
  • 1) Patients treated for childhood cancer in one of the 7 pediatric oncology
  • centres between 1960-2001.
  • 2) A histological verified diagnosis of malignancy covered by the ICCC3 and
  • including long-term survivors of severe forms of Langerhans Cell Histiocytosis
  • treated with chemotherapy and/or radiotherapy.
  • 3) Age 0-17 years at diagnosis malignancy.
  • 4) Survival at least 5 years from diagnosis.
  • Additional inclusion criteria apply for the DCOG-LATER sexual function and
  • psychosexual development study:
  • 1) Alive at time of study
  • 2) Age 18 years or older
  • 3) No severe mental retardation
  • 4) Sufficient understanding of the Dutch language to complete the
  • questionnaires.

排除标准

  • 1) Treated for childhood cancer after 2001
  • 2) less than 5 year survival from diagnosis
  • 3) age at time of study less than 18 years
  • 4) living abroad at time of study
  • 5) mental retardation
  • 6) insufficient knowledge of dutch language to complete questionnaires

研究者

发起方
Stichting Kinderoncologie Nederland

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