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临床试验/NCT04048213
NCT04048213已完成不适用

The Becoming of Children With Doose Syndrome

Centre Hospitalier Universitaire, Amiens2 个研究点 分布在 1 个国家目标入组 9 人开始时间: 2019年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
9
试验地点
2
主要终点
disease effects on the learning ability of children with doose syndrome

研究概览

简要总结

Doose syndrome is a rare epileptic syndrome that can lead to learning difficulties and a poor quality of life. The goal of this study is to evaluate the evolution of epilepsy and its consequences on cognitive development and learning issues in children with Doose syndrome.

详细描述

Doose syndrome is a rare epileptic syndrome beginning between ages two and five, characterized by myoclonic-astatic seizures which can be associated with myoclonic seizures, astatic seizures, absences and generalized tonic-clonic seizures. These seizures can be difficult to treat effectively and may lead to learning difficulties. During this study, parents of children with Doose syndrome will receive a questionnaire regarding learning disabilities, quality of life and epilepsy of their children.

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
1 Year 至 6 Years(Child)
性别
All
接受健康志愿者

入选标准

  • children with doose syndrome diagnosed between ages 1 and 6
  • normal development until onset of seizures

排除标准

  • unconfirmed diagnoses
  • abnormal diagnoses
  • abnormal psychomotor development before onset of seizures
  • cerebral MRI abnormalities
  • other child epileptic syndromes

结局指标

主要结局

disease effects on the learning ability of children with doose syndrome

时间窗: day of inclusion

disease effects on the learning ability of children with doose syndrome base on scholar informations

次要结局

  • Evolution of epilepsy in children with doose syndrome based on pathological symptoms(day of inclusion)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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