Preventive and Personalized Medicine (2021-2023)
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- genotyping for the SNP associated with hemorrhagic stroke complicating severe eclampsia in pregnancy
研究概览
简要总结
To search for a genetic marker of hemorrhagic stroke complicating severe eclampsia, a single nucleotide polymorphism (SNP) analysis of DNA obtained from the peripheral blood of patients with hemorrhagic stroke and normal control will be performed.
详细描述
Detailed Description:
Unrelated Korean subjects who have Spontaneous hemorrhagic stroke complicating severe eclampsia in pregnancy were recruited in the current study. Genotyping for various SNP associated due to the linkage disequilibrium patterns is to be performed. Genotypes would be statistically compared between patients with hemorrhagic stroke and normal control subjects free of hemorrhagic stroke
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 45 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •patients with hemorrhagic stroke complicating severe eclampsia in pregnancy
排除标准
- •patients without hemorrhagic stroke complicating severe eclampsia in pregnancy
结局指标
主要结局
genotyping for the SNP associated with hemorrhagic stroke complicating severe eclampsia in pregnancy
时间窗: 1 year
次要结局
未报告次要终点
研究者
Ildar Fakhradiyev
Head of the Laboratory of Experimental Medicine
Asfendiyarov Kazakh National Medical University