Evaluation of gastrointestinal tolerance of a new thickening powder in patients with dysphagia.
Completed
- Conditions
- Dysphagia.
- Registration Number
- NL-OMON26061
- Lead Sponsor
- umico Research B.V.Bosrandweg 20P.O. Box 70056700 CA WageningenThe NetherlandsTel. +31 (0)317-467800
- Brief Summary
Abstract geaccepteerd voor ESPEN 2007.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
Main criteria:
1. Oropharyngeal dysphagia confirmed by the SLT using bed-side swallowing evaluation or videofluoroscopy;
Exclusion Criteria
Main criteria:
1. Impaired consciousness level;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Gastrointestinal symptoms (measurements: Stool frequency & consistency, GI symptoms and food & fluid intake).<br>
- Secondary Outcome Measures
Name Time Method 1. Patient product acceptibility (intake thickening powder);<br /><br>2. Carer product evaluation (product evaluation questionnaire).