NCT05009537招募中不适用
Optical Genome Mapping in Hematological Malignancies
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 200
- 试验地点
- 4
- 主要终点
- Establish the diagnostic potential of optical genome mapping in patients with suspected hematologic cancer
研究概览
简要总结
Establish the diagnostic potential of optical genome mapping in patients with suspected hematologic cancer
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Minor/Major Patients
- •Patients with suspected hemopathies for whom we receive a sample for diagnosis in the chromosomal genetics laboratory or for whom a diagnosis of hemopathy has already been made.
- •No objection made or consent given
排除标准
- •Patients under judicial protection (guardianship, curatorship, ...),
- •Refusal to participate
结局指标
主要结局
Establish the diagnostic potential of optical genome mapping in patients with suspected hematologic cancer
时间窗: 2021-2026
identification of anomalies by mapping identical to those identified by combining conventional cytogenetics and FISH.
次要结局
- identification of new chromosomal abnormalities of clinical relevance.(2021-2026)
- identification of new chromosomal anomalies involved in oncogenic pathways(2021-2026)
研究者
研究点 (4)
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