NCT05455333Unknown不适用
Clinical Interest of a Genetic Diagnosis in Early Infant Epilepsy, Paraclinical and Therapeutic Management, and Psychological Impact of Families
University Hospital, Strasbourg, France1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2022年8月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 75
- 试验地点
- 1
- 主要终点
- Measurement of event densities
研究概览
简要总结
To determine the paraclinical and therapeutic interest of genetic diagnosis in early onset epilepsy.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- — 至 12 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Children aged ≤ 12 years,
- •hospitalized or followed at the Hautepierre Hospital of the University Hospitals of Strasbourg for primary epilepsy having started in the first 5 months of life, from 2010 to 2021.
排除标准
- •Children with secondary epilepsy (with infection trauma)
结局指标
主要结局
Measurement of event densities
时间窗: 4 month
The frequency of events (crises, going to the emergency room, hospitalizations) before and after genetic diagnosis.
次要结局
未报告次要终点
研究者
研究点 (1)
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