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临床试验/NCT01376011
NCT01376011已完成早期 1 期

Hypoxia-inducible Transcription Factor 1 (HIF-1) in Vascular Aging

Brigham and Women's Hospital2 个研究点 分布在 1 个国家目标入组 106 人开始时间: 2009年6月最近更新:
适应症

试验速览

阶段
早期 1 期
状态
已完成
入组人数
106
试验地点
2
主要终点
Define change from baseline levels of HIF-1 concentration and 3 of its regulated proteins after 6 months of quercetin (versus placebo) dietary intake.

研究概览

简要总结

The purpose of this study is to find out if quercetin can increase blood levels of hypoxia-inducible transcription factor 1 (HIF-1 protein) and to see if there is a corresponding increase in blood flow to the brain.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • healthy volunteers between the ages of 18-75 years old

排除标准

  • subjects taking vasoactive medications
  • hypertension or vascular disease
  • pregnant women
  • diabetes mellitus
  • history of seizures
  • history of stroke or head trauma
  • subjects taking digoxin, cyclosporine,felodipine, estradiol, or quinolone antibiotics
  • poor transcranial Doppler insonation windows

结局指标

主要结局

Define change from baseline levels of HIF-1 concentration and 3 of its regulated proteins after 6 months of quercetin (versus placebo) dietary intake.

时间窗: 6 months

Baseline and 6 month blood samples will be analyzed for levels of HIF-1, VEGF, EPO, and NOS

Determine change from baseline brain blood flow after 6 months of quercetin (versus placebo) dietary intake.

时间窗: 6 months

Determine cerebral vasomotor reactivity response to 6 months of quercetin intake by measuring changes in middle cerebral artery (MCA) blood flow velocity in response to changes in end-tidal CO2, and assess neurovascular coupling by measuring changes in MCA flow velocity in response to neuropsychological tasks.

次要结局

  • Define change from baseline performance in a battery of cognitive tasks after 6 months of quercetin (versus placebo) dietary intake.(6 months)

研究者

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

Farzaneh Sorond

Principle Investigator

Brigham and Women's Hospital

研究点 (2)

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