NCT06490510已完成不适用
Prognostic Significance of Mutation Type and Chromosome Fragility in Fanconi Anemia
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau1 个研究点 分布在 1 个国家目标入组 227 人开始时间: 2024年5月16日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 227
- 试验地点
- 1
- 主要终点
- Description of the clinical evolution of the patient
研究概览
简要总结
The goal of this observational study is to analyze the data included in the Spanish Registry of Patients with Fanconi anemia to better understand the natural history of the disease, identify genetic risk and prognostic factors, and identify potential therapeutic strategies.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Other
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •All patients in the Spanish Registry of Patients with Fanconi Anemia
排除标准
- 未提供
结局指标
主要结局
Description of the clinical evolution of the patient
时间窗: 1 month
Study the clinical evolution of patients with Fanconi anemia
次要结局
未报告次要终点
研究者
研究点 (1)
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