JPRN-UMIN000046189已完成Unknown
A study on the effect of continuous intake of test foods on immune function. -a randomized, placebo-controlled, double-blind, parallel-group comparison trial- - A study on the effect of continuous intake of test foods on immune function.
IMEQRD Co., Ltd.0 个研究点目标入组 100 人开始时间: 2022年11月28日最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 65years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1.Individuals who have mouth dryness, or hypersalivation. 2.Individuals who are currently undergoing treatment for any disease with medical drugs or traditional Chinese medicines. 3.Individuals who are managed by medical doctors for diet/exercise therapy. 4.Individuals who have severe diseases or a history of severe diseases. 5.Individuals who have allergic dermatitis, allergic rhinitis, bronchial asthma, or chronic bronchitis. 6.Individuals who have been taking yogurts or beverages, which include Lactic acid bacteria and/or Bifidobacterium. However, individuals who can discontinue taking these foods during the trial will be allowed. 7.Individuals who have currently been taking commercially available drugs, quasi-drug products, and foods or supplements with functional claims. However, who can discontinue taking these materials during the trial will be allowed. 8.Individuals who have a drug/food allergy. 9.Individuals who work in shift, night shift. 10.Individuals who are planning extremely change their lifestyle during the trial. 11.Individuals who drink more than 60 g alcohol/day. 12.Individuals who have been vaccinated to protect against infectious disease one month before this study. Also, planning vaccination during the trial period. 13.Individuals who are planning travel to foreign countries during the trial. 14.Individuals who are pregnant or breastfeeding. Also, planning to pregnant during the trial period. 15.Individuals who joined other clinical trials from 1 month before this trial, or those who have currently been joined or planning to join other clinical trials. 16.Individuals who donated blood more than 200 mL within one month, or more than 400 mL within three months before the screening period. 17.Individuals who cannot discontinue taking alcoholic drinks two days before the date of visit. 18.Individuals who are unsuitable for this trial, that judged by the principal investigator.
研究者
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