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临床试验/DRKS00023166
DRKS00023166已完成未知

A proof of concept study to evaluate the impact of a food supplement on production of short chain fatty acids and microbiome in healthy subjects - BTS1426/19

Evonik Operations GmbH0 个研究点目标入组 18 人开始时间: 2020年9月25日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
18

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
N/a: Single Arm Study
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 40 Years(—)
性别
Male

入选标准

  • Subject is in good physical and mental health as established by medical history, physical examination, vital signs, results of biochemistry, haematology,
  • Busy men with health unconscious eating patterns,
  • BMI: 19-30 kg/m²,
  • Non-smoker

排除标准

  • Relevant history or presence of any severe medical disorder, potentially interfering with this study
  • Subject under prescription for medication for digestive symptoms such as anti-spasmodic, laxatives and anti-diarrheic drugs or other digestive auxiliaries, use of PPIs, bismuth salts and/or H2-antagonists
  • Significant changes in lifestyle or medication (within last 3 mo.) or surgical intervention or surgical procedure such as bariatric surgery
  • Vegetarians, vegans
  • Subjects consuming food or drinks claimed as ‘probiotic’, or ‘prebiotic more than once weekly or food or drinks claimed as ‘rich in fiber’ (including specific milk products) more than 3 times per week ormore than 3 portions of fruits and vegetables (sum) per day
  • Subjects with stool frequency of = 2 stools per week
  • Subjects with history of drug, alcohol or other substance abuse, or other factors limiting their ability to co-operate during the study.
  • Relevant allergy or known hypersensitivity against compounds of the study preparations
  • Participation in another clinical study within the last 4 weeks and concurrent participation in another clinical study
  • Anticipating any planned changes in lifestyle or physical activity levels for the duration of the study

研究者

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