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临床试验/NCT00153738
NCT00153738已完成不适用

Effectiveness of Phytosterol Supplementation on Select Indices of Cardiovascular Risk

The Cooper Institute2 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2004年3月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
72
试验地点
2
主要终点
Ingestion of the supplement will result in reduced LDL cholesterol.

研究概览

简要总结

This study examined the effects of 2.6 g/d of phytosterol ingestion on LDL cholesterol metabolism. It is expected that this dose will significantly reduce LDL cholesterol after 12 weeks of supplementation.

详细描述

This study examined the effects of 2.6 g/d of phytosterol ingestion on LDL cholesterol metabolism. It is expected that this dose will significantly reduce LDL cholesterol after 12 weeks of supplementation.

The study recruited 72 men and women 20-70 years of age with mild hypercholesteremia (>130 mg/dl LDL-C). They were assigned to 1 of 2 groups. Participants ingested the supplement or a placebo for 12 weeks, with an interim assessment at 6 weeks. Participants agreed to maintain current diet, medication, and exercise habits and to not donate blood during the trial.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Prevention
盲法
Single

入排标准

年龄范围
20 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • mild hypercholesteremia, sign informed consent, not donate blood, maintain diet and exercise habits

排除标准

  • BMI <18.5 or >34.9, recent blood donation, serious or life-threatening disease

结局指标

主要结局

Ingestion of the supplement will result in reduced LDL cholesterol.

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (2)

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