ACTRN12612000389808已完成4 期
An investigation into the cognitive effects and bioavailability of components of green tea in healthy adults.
GlaxoSmithKline Nutritional Healthcare0 个研究点目标入组 51 人开始时间: 2012年4月4日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 51
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 40 Years(—)
- 性别
- All
入选标准
- •People who meet the following inclusion criteria will be included in the trial:
- •1. Male or female.
- •2. Aged 18-40 years.
- •3. Willing and able to provide written informed consent.
- •4. Understands and is willing and able to comply with all study procedures.
- •5. Are in good general health with no history of psychiatric disease.
- •6. Regular caffeine consumers (between 1-4 cups of coffee per day most days)
- •7. Must have corrected to normal vision
排除标准
- •Subjects who display any of the following will be excluded from the trial:
- •1.Females who are pregnant/lactating and/or not using a medically approved form of contraception.
- •2. Any significant concurrent illness including any bleeding disorders, heart conditions, diabetes, glaucoma, high blood pressure or osteoporosis.
- •3. Individuals who suffer from Diabetes Mellitus or diagnosed with Phenylketonuria (PKU).
- •4. Any known or suspected food allergies (this would cover all ingredients in the investigational product).
- •5. Susceptible to any unwanted side-effects of caffeine, such as reduction in sleep quality.
- •6. Smokers and users of recreational drugs (except alcohol and other food grade actives)
- •7. Have participated in any other study involving an investigational product in the last 4 weeks.
研究者
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