The Effects of Processing and Matrices on Bioavailability of Red Clover Isoflavones in Healthy Women
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 16
- 试验地点
- 2
- 主要终点
- Bioavailability of isoflavones in terms of fermented vs unfermented formulations
研究概览
简要总结
Previous literature has shown that the molecular form of isoflavones (as aglycones or glycosides) and food matrices can influence the bioavailability of these compounds in humans and hence their efficacy. To determine the effects of processing and food matrices on the bioavailability of active compounds derived from red clover the investigators will execute a 5 phase, cross-over design, open label, RCT using 20 healthy women aged between 18 to 40 years. Participants will receive 5 different formulations of red clover and bioavailability will be monitored in blood plasma using LC-MS.
详细描述
The aim of this study is to elucidate the effects food matrices and processing on the bioavailability of active compounds on the bioavailability of red clover derived isoflavones. 20 healthy participants will receive red clover derived isoflavones in five different formulations. The five formulations are split up into five phases:
Phase 1) Fermented extract in liquid form Phase 2) Fermented extract (freeze-dried) in capsule form Phase 3) Fermented extract (freeze-dried) in tablet form Phase 4) Fermented extract (concentrated) mixed in yogurt Phase 5) Un-fermented red clover in capsule or tablet form The trial will last 5-6 weeks for each participant. Plasma sample collection will take place both pre-and post- ingestion of a formulation, participants will receive blood tests at intervals -15 min, 0 min, 2hr, 4hr, 6hr, 8hr and 12hr (on the day of ingestion) and on the subsequent two mornings (24hr and 48hr) following the initiation of a phase. There will be a minimum. 5 day intervals between all phases (washout periods). Isoflavones biochanin A, formononetin, genistein and daidzein present in plasma will be detected using HPLC-MS for each phase, thus creating a bioavailability curve that can be compared to each of the other phases. The primary endpoint is to determine whether fermented extract is more bioavailable than unfermented extract.
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
- 是
入选标准
- 未提供
排除标准
- •Habitual intake of soy products, chickpeas or other supplements with a high content of isoflavones
- •Hormone therapy
- •Pregnant or breastfeeding
- •Taking drugs affecting uptake
- •Participation in other clinical trials within the last 3 months
- •Severe cardiovascular, psychiatric, neurological and / or kidney disease
- •Alcohol or substance abuse
- •Acute illness
结局指标
主要结局
Bioavailability of isoflavones in terms of fermented vs unfermented formulations
时间窗: -15min, 0hr, 2hr, 4hr, 6hr, 8hr, 12hr, 24hr, 48hr
As measured by iAUC plasma concentrations of isoflavones over 48 hours
次要结局
- Bioavailability of isoflavones in terms of matrices (tablet, capsule, yoghurt and liquid)(-15min, 0hr, 2hr, 4hr, 6hr, 8hr, 12hr, 24hr, 48hr)
研究者
Per Bendix Jeppesen
Associate Prof., PhD
University of Aarhus
