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临床试验/NL-OMON53307
NL-OMON53307已完成不适用

Dairy and Plant amino acid uptake - An explorative study - DaPa study

FrieslandCampina (FC C.V.)0 个研究点目标入组 12 人开始时间: 待定最近更新:
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

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
18 至 64(—)

入选标准

  • Apparently healthy men and women;
  • Age >=18 and <=40 years;
  • Body mass index (BMI) >=18.5 and <=30 kg/m2 ;
  • Having veins suitable for blood sampling via a catheter (judged by study
  • nurse/ medical doctor).

排除标准

  • Any self-reported metabolic, gastrointestinal, inflammatory or chronic
  • disease (such as anemia, diabetes, hepatitis, cardiovascular disease);
  • Having a history of medical or surgical events that may significantly affect
  • the study outcome, including: Inflammatory bowel disease, hepatitis,
  • pancreatitis, ulcers, gastrointestinal or rectal bleeding; major
  • gastrointestinal tract surgery such as gastrectomy, gastroenterostomy, or bowel
  • resection; known or suspected gastrointestinal disorders, colon or GI tract
  • Anaemia (Haemoglobin (Hb) values <7.5 mmol/L for women and <8.5 mmol/L for
  • men), as assessed by finger prick blood during screening visit;
  • Having a food allergy, cow*s milk protein, soy or bean protein allergy,
  • favism (G6PD-deficiency), and/or lactose intolerance (self-reported);
  • Use of glucose lowering drugs, insulin;
  • Use of medication that may impact gastric emptying (e.g. gastric acid
  • inhibitors or laxatives);
  • Use of antibiotic treatment less than 1 month before start of the study and
  • during the study;
  • Use of anti-depressives as a treatment for depression;
  • Use of protein supplements (must be stopped 1 week before the first test
  • Reported weight loss or weight gain of > 3 kg in the month prior to pre-study
  • screening, or intention to lose weight during the study period;
  • Reporting to follow or having planned a slimming or medically prescribed diet.
  • Not willing to keep a stable lifestyle during the study period;
  • Recent blood donation (<1 month prior to test day 1 of the study) or not
  • willing to stop donation during and 1 month after the study;
  • Average alcohol intake >21 (women) or >28 (men) glasses of alcoholic
  • beverages per week;
  • Use of drugs;
  • Current smokers;
  • Pregnant, lactating or wishing to become pregnant in the period of the study
  • (self-reported);
  • Not having a general practitioner;
  • Insufficient proficiency in Dutch to understand information brochure and
  • questionnaires;
  • Participation in any clinical trial including blood sampling and/or
  • administration of substances up to 30 days before test day 1 of this study;
  • Being an employee of the department Food, Health & Consumer Research of
  • Wageningen Food & Biobased Research or FrieslandCampina R&D.

研究者

发起方
FrieslandCampina (FC C.V.)

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