Establishment of Genomic and Phenotypic Database for Niemann-Pick Disease, Type C
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- Clinical data, genomic markers
研究概览
简要总结
Background:
Niemann-Pick type C (NPC) disease is a rare, progressive neurodegenerative disease that affects mainly the brain, liver, and spleen but also other parts of the body. There is no cure for NPC, and symptoms only get worse over time. Symptoms can include seizures, difficulty moving or talking, or dementia. But symptoms can vary among different people with the disease. Some may have seizures, while others do not, for example. Some people begin showing symptoms in childhood; in others, symptoms may not appear until they are adults. Researchers want to learn more about why NPC affects people differently. This natural history study will gather data from people with NPC in order to understand more about the disease and how it affects the body.
Objective:
This study will create the first and largest database about NPC.
Eligibility:
People of any age who have NPC.
Design:
Participants will have blood drawn from a vein. This will happen only once. The blood will be used to analyze the participants DNA.
The participants medical records will be reviewed. The study team will collect data on participants NPC diagnosis and symptoms; they will record how long participants have had each symptom. The study team will also collect data on each participants age, sex, race, height, weight, medications, and other test results.
The study team will communicate with participants. They will discuss the study and answer any questions.
Participants will receive up to $190.
详细描述
Study Description:
The primary objective of this protocol is to investigate the phenotypic heterogeneity of NPC by using clinical and genomic data, and to establish a comprehensive database to facilitate future investigations.
Objectives:
- Identify correlations between NPC clinical phenotypic findings and genomic markers to facilitate the understanding of the heterogeneity of this disease.
- Identify genetic contributions to NPC disease progression that can be utilized as potential therapeutic targets.
- Establish the first and largest database of genomic and phenotypic information for NPC to benefit the NPC research and patient community.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 3 Months 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •INCLUSION CRITERIA;
- •In order to be eligible to participate in this study, an individual must meet all of the following criteria:
- •Provision of signed and dated informed consent form
- •Stated willingness to comply with all study procedures and availability for the duration of the study
- •Male or female, any age, demographic or ethnic background will be eligible for this study
- •Diagnosis of NPC will be based on clinical, biochemical or molecular testing.
排除标准
- •An individual who meets any of the following criteria will be excluded from participation in this study:
- •Unwilling to provide consent
- •Unable to provide biospecimen to obtain DNA
- •Unable to provide medical records or clinical data
研究组 & 干预措施
Affected
Patients with Niemann-Pick Disease, type C
结局指标
主要结局
Clinical data, genomic markers
时间窗: 2 years
Identify correlations between NPC clinical phenotypic findings and genomic markers to facilitate the understanding of the heterogeneity of this disease.
Whole genome
时间窗: 2 years
Identify genetic contributions to NPC disease progression that can be utilized as potential therapeutic targets.
次要结局
未报告次要终点