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临床试验/NCT01010009
NCT01010009已完成不适用

Effects of Resveratrol on Cerebral Blood Flow Parameters and Cognitive Performance in Humans: a Double-blind, Placebo-controlled, Crossover Investigation

Northumbria University2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2008年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
24
试验地点
2
主要终点
Modulation of Deoxygenated Levels of Haemoglobin

研究概览

简要总结

Research shows that resveratrol is able to induce vasodilation (and therefore blood flow) by interacting with nitric oxide (NO). Research also shows that acute administration of metabolic substrates, like oxygen and glucose, can enhance aspects of cognitive performance in young, healthy humans. The aim of this investigation was to determine if the consumption of resveratrol could modulate cerebral blood flow and if this in turn could influence cognitive performance by increasing access to blood borne metabolic fuel. Results showed that compared to placebo, after consuming 500mg pure trans-resveratrol, levels of total haemoglobin were significantly higher in the frontal cortex of young, healthy participants during cognitive task completion. Cognitive performance was not effected.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Male/female,
  • Age 18-35 years old
  • Non smoker
  • Proficient in English
  • Not taking any herbal or prescription medications
  • Not pregnant
  • Does not drink more than 6 cups of coffee per day

排除标准

  • Suffered a head injury, neurological disorder or neuro-developmental disorder
  • Food allergies/intolerances

结局指标

主要结局

Modulation of Deoxygenated Levels of Haemoglobin

时间窗: 0-81 mins (absorption period=1- 45 mins , post dose period 46- 81 mins)

This outcome measure provides the change from baseline values (in µmol/L) of levels of deoxygenated haemoglobin during the 46-81 min post dose testing period. This was measured in the frontal cortex by near infrared spectroscopy (NIRS).

Modulation of Levels of Total Haemoglobin

时间窗: 0-81 mins (absorption period=1- 45 mins , post dose period 46- 81 mins)

This outcome measure provides the change from baseline values (in µmol/L) of total levels of haemoglobin during the 46-81 min post dose testing period. This was measured in the frontal cortex by near infrared spectroscopy (NIRS).

次要结局

  • Number of Participants With Significant Modulation of Cognitive Performance(46-81 mins post dose)

研究者

申办方类型
Other

研究点 (2)

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