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临床试验/NCT02089867
NCT02089867已完成2 期

A Randomized Open Label Trial to Assess the Effect of Plant Sterols Associated With Ezetimibe in LDL-cholesterol Levels in Coronary Patients Previously on Statin Therapy

Jose Rocha Faria Neto1 个研究点 分布在 1 个国家目标入组 47 人开始时间: 2006年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
47
试验地点
1
主要终点
Decrease of LDL cholesterol levels due to plant sterols associated with ezetimibe.

研究概览

简要总结

The purpose of this study is to determine the effect of plant sterols associated with ezetimibe in LDL-cholesterol levels in coronary patients previously on statin therapy

详细描述

Background: Consumption of food products enriched with plant sterols and treatment with ezetimibe both reduce cholesterol absorption in the intestine by different mechanisms and effectively reduce LDL cholesterol (LDL-c) plasma levels. Although, the associated usage of ezetimibe to plants sterols in coronary patients not reaching recommended lipid levels despite the use of statins has not yet been demonstrated. Objectives: Evaluate if ezetimibe 10mg associated to plant sterols spread enriched with 2g of plant sterols in coronary patients not reaching recommended lipid levels despite the use of statins is able to reduce cholesterol levels after 6 week treatment. Methods: Prospective, open-label study with both male and female patients with stable coronary disease and LDL > 70mg/dL. Patients will be randomized for the following 6 week treatment: control group (CT) no additional statin therapy, ezetimibe group (EZ) 10 mg/day ezetimibe, plant sterol group (PS) spread enriched with 2g of plant sterols or ezetimibe+plant sterols group (EZ+PS) 10mg/day EZ + 2g PS. Anthropometric evaluations and laboratory exams (blood glucose test, total cholesterol, LDL-c, HDL-c, triglycerides, and C-Reactive Protein) will be performed in all groups at baseline and after the sixth week intervention.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with previous myocardial infarction, stroke or coronary angiography demonstrating significant coronary disease.
  • Subjects under statin treatment with a fixed dosage for the previous three months before randomization, and did not reached LDL less than 70mg/dl.

排除标准

  • Subjects already taking ezetimibe and/or plant sterols
  • Younger than 18 years
  • Presence of any contraindication to statin
  • Pregnant women or breast-feeding women or
  • Patients with previous history of statin hypersensibility

研究组 & 干预措施

Ezetimibe

Experimental

The ezetimibe group will receive 10 mg/day ezetimibe for 6 weeks.

干预措施: Ezetimibe (Drug)

Plant sterols

Experimental

The plant sterol group will receive spread enriched with 2g daily of plant sterols for 6 weeks

干预措施: Plant sterols (Dietary Supplement)

Ezetimibe + plant sterols

Experimental

The ezetimibe + plant sterols group will receive ezetimibe 10 mg/day + spread enriched with 2g daily of plant sterols for 6 weeks

干预措施: Ezetimibe + plant sterols (Other)

结局指标

主要结局

Decrease of LDL cholesterol levels due to plant sterols associated with ezetimibe.

时间窗: 6 weeks

The primary end-point was the LDL cholesterol levels change after the plant sterols associated with ezetimibe from baseline up to 6 week treatment.

次要结局

  • Any change of non-LDL-cholesterol, total cholesterol, high-density lipoprotein (HDL), very-low-density lipoprotein (VLDL), triglycerides levels, and changes in high sensitive C reactive protein (CRP) levels.(6 weeks)

研究者

发起方
Jose Rocha Faria Neto
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Jose Rocha Faria Neto

Professor in Medicine, Pontifícia Universidade Católica do Paraná (PUCPR)

Pontifícia Universidade Católica do Paraná

研究点 (1)

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