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临床试验/NCT02116816
NCT02116816已完成不适用

Investigation Into Polyphenol Absorption Profiles

Hull University Teaching Hospitals NHS Trust2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2014年4月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
2
主要终点
Area Under the Absorption Curve for each polyphenol preparation

研究概览

简要总结

This study consists of two parts. The first part of the study looked at the absorption of three different polyphenol preparations into the blood, the variability of their absorption and whether their absorption could be enhanced by mixing with pollen shells. For this purpose 12 healthy volunteers were recruited. All participants received all the 3 supplements with and without mixing with pollen shells so they had a total of 3 tests. For each test six blood samples were taken over an 8 hour period. Urine samples were also collected.

Oligopin was selected from the first study. The second part of study aims to look at the effects of Oligopin on endothelial function by assessing vascular tone and function in healthy volunteers using a non-invasive, direct measurement of vasodilatory capacity (EndoPAT). Nitrate and nitrite measurements, as well as blood pressure measurements, will also be recorded to provide a clear clinical assessment of the effects of this preparation (if any) upon vascular function. The effects of Oligopin will be compared to a placebo (methylcellulose-filled capsules) to allow a robust assessment of any clinical effects. A total of 24 healthy volunteers will be recruited for this study.

详细描述

This study consists of two parts. The first part of the study looked at the absorption of three different polyphenol preparations into the blood, the variability of their absorption and whether their absorption could be enhanced by mixing with pollen shells (pollen shells have been shown to enhance lipid molecule absorption). For this purpose 12 healthy volunteers were recruited. All participants received all the 3 supplements with and without mixing with pollen shells so they had a total of 3 tests. For each test six blood samples were taken over an 8 hour period. Urine samples were also collected.

Oligopin was selected from the first study. The second part of study aims to look at the effects of Oligopin on endothelial function by assessing vascular tone and function in healthy volunteers using a non-invasive, direct measurement of vasodilatory capacity (EndoPAT). Nitrate and nitrite measurements, as well as blood pressure measurements, will also be recorded to provide a clear clinical assessment of the effects of this preparation (if any) upon vascular function. The effects of Oligopin will be compared to a placebo (methylcellulose-filled capsules) to allow a robust assessment of any clinical effects. A total of 24 healthy volunteers will be recruited for this study.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
盲法
None

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

  • Male or Female subjects between the age of 18-65 who can speak and understand English
  • No concomitant medication including herbal medicines and food supplements
  • No concomitant disease processes
  • Body Mass Index 21- 29kg/m2
  • Systolic blood pressure ≤150 mm Hg and diastolic pressure <90 mm Hg
  • Subjects who have given informed consent

排除标准

  • Patients not wishing to allow disclosure to their GPs.
  • Concomitant medication including herbal medicines and food supplements
  • Concomitant disease processes
  • History of drug/alcohol abuse or Alcohol intake within 24 hours of dosing visit (visits 2-4)
  • Body Mass Index <21 and > 29kg/m2
  • Systolic blood pressure >150 mm Hg and or a diastolic pressure>90 mm Hg
  • Unable to tolerate polyphenol products or adhere to low polyphenol diet
  • Subjects not willing or able to fast until 12 noon (a total of 14 hours).
  • Pregnant females or planning to conceive in the next 3 months.
  • Participation in any other study currently or in the last three months.

研究组 & 干预措施

Polyphenol

Experimental

Polyphenol preparations

干预措施: Polyphenol (Dietary Supplement)

结局指标

主要结局

Area Under the Absorption Curve for each polyphenol preparation

时间窗: 8 hours

Blood samples will be withdrawn 6 times over an 8 hour period: baseline, then 30 minutes, 1 hour, 2 hours, 4 hours and 8 hours after ingestion of each polyphenol supplement (total 3 supplements)

次要结局

未报告次要终点

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (2)

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