NCT02831647已完成不适用
Tolerance and Acceptability of AYMES PRAGUE
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 20
- 主要终点
- GI side effects when using AYMES PRAGUE
研究概览
简要总结
Tolerance and Acceptability of new oral nutritional supplement - AYMES PRAGUE
详细描述
To evaluate tolerance and acceptability of AYMES PRAGUE in patients requiring supplementary oral nutritional support compared with currently available alternatives, measuring outcomes of GI effects, Compliance, product preference,convenience etc.
To obtain data to support an ACBS submissions for AYMES PRAGUE (to allow for prescription in the community at NHS expense).
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 100 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Adult patients (≥18 years) who are able to communicate their views regarding acceptability.
- •Patients established on an oral nutritional supplement, being prescribed 1-2 ONS providing approximately 300kcal/day
- •Patients expected to require oral nutritional supplementation for at least 2 further weeks.
- •Informed consent obtained.
排除标准
- •Participation in any other studies involving investigational or marketed products concomitantly or within two weeks prior to entry into the study
- •Patients requiring a milk-free diet
- •Patients with medical or dietary contraindication to any feed ingredients (see appendix 2 of protocol for full list)
- •Patients with significant renal or hepatic impairment
- •Patients with swallowing impairment requiring thickened fluids
- •Patients with inflammatory bowel disease or previous bowel resection.
结局指标
主要结局
GI side effects when using AYMES PRAGUE
时间窗: 9 DAYS
Recording of absence/presence of any nausea, vomiting, abdominal pain, bloating / flatulence, when using AYMES PRAGUE as assessed by presence / absence of side effect compared to baseline period
次要结局
- Bowel habits of subjects when using AYMES PRAGUE - stool consistency(9 days)
- Change to bodyweight of subjects when using AYMES PRAGUE(9 days)
- Bowel habits of subjects when using AYMES PRAGUE - frequency(9 days)
- Compliance with prescription of AYMES PRAGUE(9 days)
研究者
相似试验
已完成
不适用
Acceptability and Tolerance Study of a New Oral Nutritional Supplement (ONS)MalnutritionNCT02898038Aymes International Limited16
已完成
不适用
Acceptability and Tolerance of New Oral Nutritional SupplementMalnutritionNCT02639156Aymes International Limited22
已完成
不适用
Acceptability and Tolerance Study of New Oral Nutritional SupplementMalnutritionNCT02648451Aymes International Limited17
已完成
不适用
Tolerance and Acceptability Evaluation of AYMES AMSTERDAMMalnutritionNCT04700293Aymes International Limited18
已完成
不适用
Tolerance and Acceptability Evaluation AYMES ActaGainMalnutritionNCT04703881Aymes International Limited17