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临床试验/NCT00312923
NCT00312923已完成2 期

Preliminary Study of Safety and Efficacy of Policosanol

Rush University Medical Center1 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2005年9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
入组人数
54
试验地点
1
主要终点
LDL Cholesterol

研究概览

简要总结

Lay Language Summary: High cholesterol levels are common in persons with HIV infection. However, conventional cholesterol-lowering medications may have harmful side effects when given to HIV-infected persons. Therefore, we plan to evaluate the safety and effectiveness of policosanol, a dietary supplement derived from sugar cane that has cholesterol-lowering properties, to lower cholesterol levels in persons with HIV infection. We hypothesize that policosanol will lower levels of LDL cholesterol ("bad" cholesterol) and raise levels of HDL cholesterol ("good" cholesterol).

详细描述

As per Brief Summary

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • CD4 count > 250 Plasma HIV RNA < 50,000 Currently receiving HAART age 18-60 total cholesterol between 200-240 or triglycerides between 150-400 or LDL cholesterol > 160

排除标准

  • kidney or liver disease current use of lipid-lowering drugs pregnancy lactation

研究组 & 干预措施

Policosanol

Experimental

20 mg daily of policosanol

干预措施: Policosanol (Drug)

Placebo

Placebo Comparator

20 mg of microcrystalline cellulose daily

干预措施: Placebo (Dietary Supplement)

结局指标

主要结局

LDL Cholesterol

时间窗: 12 weeks

Low density lipoprotein cholesterol

次要结局

  • Triglycerides(12 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Barbara Swanson

Assistant Professor

Rush University Medical Center

研究点 (1)

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