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临床试验/NCT04796259
NCT04796259已完成不适用

Malt-derived Ingredients and Their Prolactinotrophic Effects

Société des Produits Nestlé (SPN)2 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2021年2月5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
12
试验地点
2
主要终点
Prolactinotrophic effect

研究概览

简要总结

This proof-of-concept study aims to investigate whether malt-derived ingredients have acute prolactinotrophic effects in healthy women of child-bearing age.

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
None

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Subjects who have/are
  • Willing and able to provide written informed consent
  • Healthy women aged 18 to
  • BMI in the range of 18 to
  • Willing to undergo an experiment in the follicular phase of the menstrual cycle i.e. day 0 to 14 of the menstrual cycle starting from the first day of the period.

排除标准

  • Subjects who have/are
  • Allergic to tested products
  • Under regular medication including oral contraceptive pills or other form of hormonal replacement therapy.
  • Under medications which affects prolactin levels.
  • Pregnant or lactating or planning to conceive during the study period.
  • Smokers, or excessive alcohol consumption (alcohol intake higher than 2 servings per day. A serving is 0.4 dl of strong alcohols, 1 dl of red or white wine, or 3 dl of beer) or other substance abuse.
  • Not willing and/or not able to comply with the study procedures and requirements.
  • Suffering from pre-existing medical conditions and chronic illnesses that in the opinion of the investigator may interfere with the study.
  • Family or hierarchical relationships with research team members

结局指标

主要结局

Prolactinotrophic effect

时间窗: 2 hours post consumption

Δ of serum Prolactin Cmax between test products, positive control of beer solids and negative control of still water

次要结局

  • Gastrointestinal tolerability(2 hours post consumption)

研究者

发起方
Société des Produits Nestlé (SPN)
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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