TCTR20240409003招募中不适用
A study of the incidence of molecular mutations in newly diagnosed acute lymphoblastic leukemia (ALL) patients by Next-generation sequencing technique
Siriraj Hospital Mahidol University0 个研究点目标入组 140 人开始时间: 2024年4月9日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 140
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 Years 至 N/A (No limit)（—）
- 性别
- All
入选标准
- •1.A retrospective cohort: Thai newly diagnosed ALL patients
- •2.A prospective cohort: Thai newly diagnosed ALL patients aged greater than 18 years who had genetic workup results by NGS study and signed informed consent OR
排除标准
- •Poor quality specimen from a protocol number 388/2561(EC2)
研究者
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