NCT01801488终止不适用
Genome-wide Analysis of Single Nucleotide Polymorphisms of Brain Arteriovenous Malformations and Cerebral Aneurysm
State University of New York - Upstate Medical University1 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2011年11月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 发起方
- 入组人数
- 5
- 试验地点
- 1
- 主要终点
- Risk gene expression
研究概览
简要总结
Test single nucleotide polymorphisms (SNP's) in ruptured and unruptured aneurysm tissue to identify a genetic difference between the two types of aneurysms; and to test SNP's in arteriovenous malformation tissue to identify a genetic link.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 89 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •All adult patients between the ages of 18 and 89 that are having open surgical resection of an AVM or clipping of an aneurysm will be included
排除标准
- 未提供
结局指标
主要结局
Risk gene expression
时间窗: Within one week of sample collection.
The samples will be frozen after collection and then analyzed.
次要结局
未报告次要终点
研究者
研究点 (1)
Loading locations...
相似试验
已完成
不适用
Genetic Polymorphism and Parkinson's Disease in TaiwaneseParkinson's DiseaseNCT01996878Changhua Christian Hospital334
已完成
不适用
The Occurrence of Single Nucleotide Polymorphism Among Women Who Experienced Obstetric Anal Sphincter InjuryDelivery, ObstetricNCT04047433HaEmek Medical Center, Israel93
撤回
不适用
Protocol for Postmenopausal Women at Increased Risk of Developing Breast CancerBreast CancerNCT00329017Carol Fabian, MD
已完成
不适用
Investigation of Genetic Disease Marker Associated With Korean Glaucoma PatientsSingle-nucleotide Polymorphism (SNP) for GlaucomaNCT01025024Chungnam National University1,224
已完成
不适用
Genetics of Aortic Stenosis: From Family Forms to the Common FormsAortic StenosisNCT02890407Nantes University Hospital1,987