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临床试验/NL-OMON37491
NL-OMON37491招募中不适用

Hereditary breast cancer and the clinical significance of variants in the BRCA1 and BRCA2 genes. - Hereditary breast cancer and DNA Unclassified Variants.

eids Universitair Medisch Centrum0 个研究点目标入组 270 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
270

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

  • 1) UV-cohort: patients who are carrier of an unclassified variant.
  • 2) Affected relatives of the UV-cohort patients will be invited for this study.
  • 3) At least one non-affected family member of the UV-cohort patients will be invited to take part in this study. ;The UV-cohort consists of patients diagnosed with a primary breast tumor before the age of 60 years and are unrelated.
  • The patient can be included if only one unclassified variant is found in the BRCA1 or BRCA2 gene.
  • All the participants should be older than 18 years, competent and independent of the researcher.
  • They should all be informed about the study, its goal and its duration.
  • They know about the possibility of interim quitting the study.

排除标准

  • - Younger than 18 years old and older than 60 years old. Not affected family members may however, be older than 60 years old.
  • -The participants should be competent to be able to make decision about participation.

研究者

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