NL-OMON36348已完成2 期
Gastric versus distal to the ligament of Treitz feeding in healthy volunteers - GuTz study
Danone Research - Centre for Specialised Nutrition0 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
- 2 期
- 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 99(—)
入选标准
- •Age range: 18 - 45 years
- •Understanding of the Dutch language
- •BMI range: 18 - 27 kg/m2
- •Functioning gastrointestinal tract, eligible for tube feeding via an intestinal tube
- •Willingness to comply with the study protocol, including:
- •- Use of standard breakfast day 1 of visit 1 and 2
- •- Refrain from alcohol consumption 48h prior to, and during the assessments
- •- Refrain from intense physical activities 48h prior to, and during the assessments
- •- Refrain from antibiotics, NSAID*s and vitamins 2 weeks prior to, and during the assessments
- •- Refrain from fish oil 4 weeks prior to, and during the assessments
- •Written informed consent
排除标准
- •Any relevant gastrointestinal medical history, e.g.:
- •- Major gastrointestinal surgery
- •- Gastrointestinal disease, e.g.:
- •- Gastric or paraesophagal hernia
- •- Gastrointestinal obstruction
- •- Heartburn
- •Diabetes mellitus type I and II
- •Hepatic or renal pathology
- •Any relevant results of physical exam during screening; defined as:
- •- Diastolic blood pressure >=130mmHg
- •- Abnormal heart souffle
- •- Heart rhythm disorder
- •- Abnormal respiratory sounds
- •Any results of laboratory tests during screening other than the normal limit defined by the laboratory (Medial)
- •Any relevant exclusion criteria listed on the product label; e.g.:
- •- Subjects requiring a fibre-free diet
- •Allergy / intolerance for the enteral nutrition
- •Allergy / intolerance for contrast given during the abdominal X-ray
- •Smoking, alcohol abuse; defined as:
- •- Currently smoking or quit <=6 months ago
- •- > 21 units of alcohol a week
- •Donor of blood the last 6 months
- •Any other medical condition that may interfere with the safety of the subjects or the outcome parameters, in the investigator*s judgment
- •Investigator's uncertainty about the willingness or ability of the subject to comply with the protocol instructions
- •Participation in any other studies involving investigational or marketed products concomitantly or within two weeks prior to entry into the study
研究者
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