NCT02065817已完成不适用
Dose of Labeled Cholesterol and Phenylalanine for HDL Kinetics: A Pilot Study
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Mayo Clinic
- 入组人数
- 7
- 试验地点
- 1
- 主要终点
- Incorporation of orally administered 13C3 cholesterol into plasma cholesterol
研究概览
简要总结
This is a pilot study to determine the optimum time and dose to draw blood samples using a tracer for HDL kinetics.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Basic Science
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 50 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Healthy men and women ages 18 - 50
排除标准
- •Cardiovascular disease
- •Metabolic disease
- •Hematologic disorder
- •Liver or kidney disease
- •phenylketonuria
- •Currently taking lipid lowering medications or any other drugs that could affect lipid metabolism
研究组 & 干预措施
Tracer
Experimental
干预措施: stable isotope of cholesterol (Other)
结局指标
主要结局
Incorporation of orally administered 13C3 cholesterol into plasma cholesterol
时间窗: 72 hours
13C3 cholesterol, which is labeled with a stable isotope, will be administered orally. Blood samples will be taken every 4-6 hours for 72 hours for the measurement of stable isotopic enrichment in cholesterol using gas chromatography-mass spectrometry. The study has a dual purpose: to determine the optimum oral dose of isotope, and to determine the time of peak enrichment in plasma cholesterol.
次要结局
未报告次要终点
研究者
研究点 (1)
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