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临床试验/NCT01141777
NCT01141777已完成不适用

The Effects of Spirulina Platensis on Insulin Resistance in HIV-infected Patients

Yaounde Central Hospital1 个研究点 分布在 1 个国家目标入组 33 人开始时间: 2008年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
33
试验地点
1
主要终点
Percentage difference in change in insulin sensitivity between the two groups at the end of eight weeks of intervention

研究概览

简要总结

Spirulina, a widely used food supplement, improves the lipid profile and glycemic control in people living with diabetes, suggesting that it could have some effects on insulin sensitivity. Since HIV-infected patients develop metabolic abnormalities due to the virus and/or to antiretroviral (ARV) drugs, the investigators therefore proposed to evaluate the effect that spirulina can have on HIV/HAART-associated insulin resistance

详细描述

Even though antiretroviral therapy (ART) has dramatically improved the health of people living with HIV/AIDS, the prospect of maintaining patients long term on ART can be severely restricted by the development of serious long term effects in their metabolism. These abnormalities include dyslipidemia, lipodystrophy and disorders of glucose metabolism with insulin resistance believed to be the underlying pathophysiological mechanism.

Spirulina, has recently drawn attention on its cholesterol and blood pressure lowering effects, including improvement of glycaemic control in diabetics subjects, suggesting it can have some effects on insulin sensitivity.

The aim of this three month, experimental, prospective, randomised trial was to evaluate the effect of Spirulina on HIV/HAART-associated insulin resistance on 33 subjects. Primary outcome was change in insulin sensitivity during the trial, over two time periods; t=0 and t=12 weeks. The second objective was to compare between the two groups, the percentage of subjects who improved insulin sensitivity by the end of the study.

Recruitment started in October 2008 and the trial ended in February 2009.

研究设计

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

入排标准

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

入选标准

  • Confirmed HIV infection
  • Accepted to participate in the study

排除标准

  • Acute intercurrent infection
  • Treatment that modifies glucose or lipid profile
  • Pregnancy
  • Known diabetic patient
  • Chronic renal failure with calculated creatinine clearance < 60ml/min

结局指标

主要结局

Percentage difference in change in insulin sensitivity between the two groups at the end of eight weeks of intervention

时间窗: t=0 (baseline), t= week 12 (end of trial)

次要结局

  • Percentage of subjects who improved insulin sensitivity by the end of the study, compared between the two groups(t=0 (baseline), t= week 12 (end of trial))

研究者

发起方
Yaounde Central Hospital
申办方类型
Other Gov

研究点 (1)

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