NL-OMON56237已完成不适用
Amino acid concentrations in serum after intake of plant based protein sources - Plantino I and II
utricia Research0 个研究点目标入组 32 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
- 32
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
- •1. Age >= 18 and <= 70 years
- •2. Body Mass Index (BMI) >= 18.5 and <= 27.0 kg/m2
- •3. Written informed consent
- •4. Willingness and ability to comply with the protocol
- •5. Judged by the Investigator to be in good health
排除标准
- •1. Any gastrointestinal (GI) disease or surgery that may interfere with GI
- •function and/or protein metabolism, including but not limited to
- •phenylketonuria, pancreatitis, short bowel syndrome, celiac disease, Crohn*s
- •disease, in the opinion of the Investigator
- •2. Known renal or hepatic diseases that may interfere with protein metabolism,
- •including but not limited to acute hepatitis, chronic liver disease, nephritis,
- •cystinuria, chronic kidney disease, in the opinion of the Investigator
- •3. Use of systemic medication within the past 3 weeks prior to screening which
- •in the opinion of the Investigator may influence gastric acid production and/or
- •gastrointestinal motility or function and/or protein metabolism (for example:
- •antibiotics, anticonvulsants, prokinetics, antacids, opioid analgesics,
- •anticoagulants, corticosteroids, laxatives, growth hormone, testosterone,
- •immunosuppressants, or insulin).
- •4. Allergy to soy, pea and/or cow*s milk protein
- •5. Adherence to a weight loss program
- •6. Current eating disorder, e.g. anorexia nervosa or bulimia
- •7. Known pregnancy and/or lactation
- •8. Current smoking or stopped smoking for < 1 month prior to screening (except
- •for incidental smoking of <= 3 cigarettes/cigars/pipes per week on average in
- •the last month prior to screening)
- •9. Average alcohol use of > 21 glasses per week for men or > 14 glasses per
- •week for women (on average during the last 6 months prior to screening)
- •10. Drug or medicine abuse in opinion of the investigator
- •11. Any known bleeding disorder
- •12. Known difficulties with placement of and/or blood drawings from a cannula
- •13. Active participation in any other study with investigational or marketed
- •products concomitantly or within 4 weeks prior to screening
- •14. Major medical or major surgical event requiring hospitalization within the
- •preceding 3 months and/or scheduled in the period of study participation
- •15. Investigator*s uncertainty about the willingness or ability of the subject
- •to comply with the protocol requirements
- •16. Employees of Nutricia Research and/or their family members or relatives
研究者
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