NCT02849977已完成不适用
Genetic Testing and Phenotypic Characterization of Severely Obese Pediatric and Adult Volunteers
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 5,966
- 试验地点
- 57
- 主要终点
- Identification of individuals with POMC, LepR or PCSK1 genetic mutations
研究概览
简要总结
The purpose of this screening study is to identify people who have a rare genetic cause of obesity - specifically three genetic variants (a change in the DNA structure) of the POMC, PCSK1 and LepR genes that are currently known to result in obesity.
This screening study will not include any investigational drugs. You will be asked to provide a DNA sample and answer some questions about your medical history and hunger.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Prospective
入排标准
- 年龄范围
- 2 Years 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
结局指标
主要结局
Identification of individuals with POMC, LepR or PCSK1 genetic mutations
时间窗: 1 Year
次要结局
未报告次要终点
研究者
研究点 (57)
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