NL-OMON44562已完成不适用
PARROT-2: Postprandial plasma amino acid concentrations after dairy consumption - PARROT-2
FrieslandCampina Research0 个研究点目标入组 20 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
- 20
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 99（—）
入选标准
- •- Age 18-65y
- •- BMI 18,5-30 kg/m2
- •- Non-smoking
- •- Healthy as assessed by the NIZO lifestyle and health questionnaire (Verklaring leefgewoonten en
- •gezondheid) and according to the judgment of the study physician.
- •- Regular and normal Dutch eating habits as assessed by the NIZO lifestyle and health questionnaire (3 main meals per day)
- •- Veins suitable for cannulation (blood sampling)
- •- Voluntary participation
- •- Having given written informed consent
- •- Willing to comply with study procedures
- •- Accept use of all encoded data, including publication, and the confidential use and storage of all data for 15 years.
- •- Accept disclosure of the financial benefit of participation in the study to the authorities concerned
排除标准
- •- Participation in any clinical trial including blood sampling and/or administration of substances up to 30 days before Day 01 of this study
- •- 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 cancer
- •- Use of the following medication: glucose lowering drugs, insulin; medication that may impact gastric emptying (e.g. gastric acid inhibitors or laxatives)
- •- Diagnosed with diabetes, being treated for high blood glucose or increased fasting blood glucose (> 7 mmol/l in finger prick blood) as assessed during screening visit
- •- For men: Hb <8,5 mmol/l as assessed during screening visit; for women: Hb <7,5 mmol/l.
- •- Use of protein supplements
- •- Mental status that is incompatible with the proper conduct of the study
- •- A self-reported reported food allergy or sensitivity to dairy ingredients
- •- A self-reported allergy or sensitivity to acetaminophen
- •- Alcohol consumption > 28 units/week and 4/day
- •- Reported unexplained 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
- •- Reported slimming or medically prescribed diet
- •- Recent blood donation (<1 month prior to Day 01 of the study)
- •- Not willing or afraid to give up blood donation during the study
- •- Personnel of NIZO food research or Wageningen University, department of Human Nutrition, their partner and their first and second degree relatives
- •- Not having a general practitioner
- •- Not willing to accept information-transfer concerning participation in the study, or information regarding his health, like laboratory results and eventual adverse events to and from his general practitioner
- •-Pregnancy or lactating
研究者
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