ISRCTN86521801已完成不适用
Evaluation of gastrointestinal tolerance of a new thickening powder in patients with dysphagia
umico Research BV (Netherlands)0 个研究点目标入组 50 人开始时间: 2006年2月14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
- 50
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. Oropharyngeal dysphagia confirmed by the SLT using bed-side swallowing evaluation or videofluoroscopy
- •2. Neurogenic aetiology or caused by muscle weakness
- •3. Stable severity (require thickend drinks for at least 3 weeks after inclusion)
- •4. Written informed consent
排除标准
- •1. Impaired consciousness level
- •2. Inadequate cognitive skills to comprehend study requirements and to communicate responses to questions
- •3. Bowel habit unable to be defined using the study specific gastrointestinal (GI) questionnaire
- •4. Enteral tube feeding corresponding to >50% of total energy intake
- •5. Use of any foods or fluids thickened with another commercial thickener
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