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.
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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