ISRCTN51742545已完成不适用
The effect of intraileal infusion of fat emulsions, differing in degree of saturation, on satiety and food intake after a liquid meal replacement
eiden University Medical Centre (LUMC) (Netherlands)0 个研究点目标入组 15 人开始时间: 2006年1月27日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 15
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
- 性别
- All
入选标准
- •1. Signed informed consent form
- •2. Sex: male or female
- •3. Age: 18 - 55 years
- •4. Body mass index (BMI): 18 - 32 kg/m^2
排除标准
- •1. Evidence of severe cardiovascular, respiratory, urogenital, gastrointestinal/ hepatic, hematological/immunologic, HEENT (head, ears, eyes, nose, throat), dermatological/connective tissue, musculoskeletal, metabolic/nutritional, endocrine, neurological/psychiatric diseases, allergy, major surgery and/or laboratory assessments which might limit participation in or completion of the study protocol
- •2. Gastrointestinal or hepatic disorders influencing gastrointestinal absorption or transit
- •3. The use of psychotropic drugs, including: benzodiazepines or alcohol in excess of 21 units/week for males and 14 units/week for females
- •4. Concomitant medication that can increase gastric pH (e.g. antacids, protonpump-inhibitors, prostaglandins, anticholinergic agents, H2-receptor antagonists), or alter gastric emptying (e.g. metoclopramide, cisapride, domperidone and erythromycin, anticholinergics, tricyclic antidepressants, narcotic analgesics, adrenergic agents, calcium channel blockers), or alter intestinal transit (e.g. loperamide, chemical/osmotic/bulk laxatives), or influence satiety/energy intake (e.g. sibutramine, glucocorticoids, anabolic steroids)
- •5. Intolerance of Slim Fast product or of ingredients of the ad libitum meal
- •6. Pregnancy, lactation, wish to become pregnant during study, or having a positive pregnancy test at inclusion
- •7. Reported unexplained weight loss/gain of more than 2 kg in the month before the study enrolment
研究者
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