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临床试验/NCT02656095
NCT02656095已完成不适用

Lipoprotein Lipase Enzyme Activity Assay Validation and Clinical Assessment

University of Colorado, Denver0 个研究点目标入组 12 人开始时间: 2016年3月最近更新:
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试验速览

阶段
不适用
状态
已完成
入组人数
12
主要终点
Evaluation of Lipoprotein lipase levels

研究概览

简要总结

This study plans to learn more about measuring Lipoprotein lipase (LPL) activity in humans. LPL is an enzyme in the breakdown of certain types of fats into smaller parts. Lipoprotein lipase deficiency (LPLD) is a very rare genetic disorder in which lipoprotein enzyme is no longer functional. This can cause conditions known as high triglycerides in the blood and inflammation of the pancreas.

Investigational medications to treat LPLD are currently being developed. In order to see if these medications are effective, it is necessary to be able to accurately measure LPL activity in humans.

LPL activity has been successfully measured in animal models after giving heparin. Heparin is a blood thinner which is approved by the FDA. It is originally used to prevent blood clots. This study will administer heparin to healthy adults through intravenous infusion (IV). Blood samples will be collected before and after the infusion to test LDL levels.

The purpose of this study is to develop a cheap, more reliable standard for assessment of LPLD in patients

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
20 Years 至 39 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • male and females between ages of 20-39

排除标准

  • Past history of LPL deficiency
  • Hypercholesterolemia (Cholesterol >200, LDL >160, HDL <35) hypertriglyceridemia (TG>150), any familial lipid disorder
  • Diabetes mellitus (type 1 or 2)
  • Uncontrolled hypertension SBP>140, DBP>90
  • History of hemorrhagic stroke
  • Current pregnancy
  • History of major surgery, invasive procedure or trauma within the last 30 days, or planned major surgery within 30 days after participating in the study
  • Exposure to heparin (unfractionated heparin or low molecular weight heparin) within 30 days prior to screening
  • History of allergy to heparin
  • History of heparin-induced thrombocytopenia
  • Current smoking
  • Active ulcerative or angiodysplastic GI diseases
  • Thrombocytopenia or platelet disorders (Platelet count <100,000/UL)
  • Major health issues which may affect the safety of study subject, including but not limited to:
  • History of chronic kidney disease (eGFR<60)
  • Long term use of medications which alter lipid metabolism
  • History of hepatic disease (ALT or AST more than 2 times the upper limit of normal)
  • History of clotting disorders, any type of coagulation factor deficiency, or thrombocytopenia
  • Chronic use of ASA, anticoagulants, platelet inhibitors
  • Use of NSAIDS for more than 2 weeks prior to screening
  • Anemia (hemoglobin <13 g/dL)

结局指标

主要结局

Evaluation of Lipoprotein lipase levels

时间窗: 10-15 minutes post-heparin adminstration

Blood will be drawn after IV heparin administration and run through assay to determine lipoprotein lipase levels.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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