NCT02704260已完成不适用
Endofibrose Vasculaire et génétique
University Hospital, Angers2 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2016年3月2日最近更新:
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 5
- 试验地点
- 2
- 主要终点
- Presence of mutations or nucleotides variations
研究概览
简要总结
search for a genetic cause of vascular endofibrose
详细描述
Perform a DNA analysis to mark the existence of mutations in one or more genes encoding proteins involved in vascular remodeling high.
5 patients or relatives of patients topics
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •High level reached Cyclists vascular endofibrose
- •Cyclist high level and not sick with a brother or sister is senior cyclist reaches the vascular endofibrose.
排除标准
- •not obtaining consent
研究组 & 干预措施
GENETIC ANALISYS
Experimental
GENETIC ANALYSIS AND RESEARCH OF GENETIC BLOOD SAMPLE
干预措施: GENETIC ANALYSIS (Genetic)
结局指标
主要结局
Presence of mutations or nucleotides variations
时间窗: 1 hour
DNA analysis and search for genetic mutations
次要结局
未报告次要终点
研究者
研究点 (2)
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