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临床试验/NCT01678521
NCT01678521已完成不适用

Effect of LDL-apheresis on Pentraxin3 Plasma Levels in Hypercholesterolemic Patients With Coronary Artery Disease

Universita di Verona1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2012年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
12
试验地点
1
主要终点
acute change in PTX3 plasma values

研究概览

简要总结

Inflammation plays a major role in atherosclerosis. Pentraxin 3 (PTX3) a multifunctional pattern-recognition protein, is expressed in many tissues/cells, including innate immunity cells, endothelium and atherosclerotic plaques. Its role is controversial: it may exert protective cardiovascular effects and/or it may be an indicator of plaque vulnerability and future cardiovascular risk.

LDL-Apheresis removes apoB100-containing lipoproteins and it can prevent progression of coronary artery disease (CAD). LDL-Apheresis exerts non-lipidic beneficial effects on the procoagulatory state and on hemorheology. No data exist about the effects of LDL-Apheresis on plasma PTX3 levels.

详细描述

Hypercholesterolemic patients with documented CAD, on chronic fortnightly LDL-apheresis treatment will be enrolled in this study.

Blood samples will be collected before and after a single LDL-Apheresis treatment to asses PTX3, HsCRP, IL6, IL10, Fibrinogen and lipid plasma levels.

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
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Hypercholesterolemia
  • documented CAD
  • chronic LDL-apheresis treatment

排除标准

  • mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation

结局指标

主要结局

acute change in PTX3 plasma values

时间窗: before and at the end of one LDL-apheresis treatment (about 6 hours)

blood samples will be collected before and after a single LDL-apheresis treatment

次要结局

  • acute change in hsCRP(before and at the end of one LDL-apheresis treatment (about 6 hours))
  • acute change in IL6 and IL10(before and at the end of one LDL-apheresis treatment (about 6 hours))

研究者

发起方
Universita di Verona
申办方类型
Other
责任方
Principal Investigator
主要研究者

Maria Grazia Zenti

principal investigator

Universita di Verona

研究点 (1)

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