NCT01536821已完成不适用
PROGENI (Parkinson's Research: The Organized Genetics Initiative) Family Study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 81
- 试验地点
- 10
- 主要终点
- Observation and biological specimen collection
研究概览
简要总结
The PROGENI Family Study is part of a larger consortium that is studying a gene shown to be important in Parkinson's disease, called LRRK2. People who have a defect in the LRRK2 gene will often develop Parkinson's disease. Eligible participants will be asked to complete a single Study Visit at an affiliated research facility closest to their home.
详细描述
Participants will be asked to complete a family history questionnaire, which will gather information about their family history of Parkinson's disease and related disorders. They will be asked to complete a single Study Visit, during which they will be asked to do some or all of the following:
- Complete questionnaires regarding Parkinson's disease symptoms, medical history, mood, sleep, mental status, and activity level.
- Be given a brief standard neurological examination.
- Be given a scratch and sniff smell identification test.
- Be asked to give a sample of approximately 2 tablespoons of blood.
- Be asked to give a urine sample of approximately 1 tablespoon of urine.
研究设计
- 研究类型
- Observational
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Positive for a LRRK2 mutation
排除标准
- 未提供
结局指标
主要结局
Observation and biological specimen collection
时间窗: 1 time
次要结局
未报告次要终点
研究者
研究点 (10)
Loading locations...
相似试验
已完成
不适用
Parkinson's Research: The Organized Genetics InitiativeParkinson DiseaseNCT00086073Indiana University School of Medicine1,800
终止
不适用
Parkinson's Disease Genetics DatabaseParkinson's DiseaseNCT00855556Northwell Health16
已完成
不适用
Molecular Epidemiology of Parkinson's DiseaseParkinson DiseaseNCT00042107National Institute of Environmental Health Sciences (NIEHS)2,022
已完成
不适用
Web-based Genetic Research on Parkinson's DiseaseParkinson's DiseaseNCT0135146723andMe, Inc.13,576
已完成
不适用
Research of Biomarkers in Parkinson DiseaseProgressive Supranuclear PalsyDiffuse Lewy Body DiseaseParkinson DiseaseHuntington DiseaseMultiple System AtrophyDystoniaNCT00465790Institut National de la Santé Et de la Recherche Médicale, France219