AAA study
- Conditions
- Healthy older subjects (age 65 years or older)
- Registration Number
- NL-OMON22155
- Lead Sponsor
- utricia Research B.V.
- Brief Summary
ot applicable
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 13
Inclusion Criteria
1. Age 65 years or older
2. BMI from 20 through 30 kg/m2
Exclusion Criteria
1. Any gastrointestinal (GI) disease or surgery that interferes with GI function
2. Known renal or hepatic failure
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome parameter in this study is the time to reach half incremental area under the curve (t½ iAUC) for the sum of all amino acids (total AA) comparing product A to product B.
- Secondary Outcome Measures
Name Time Method The secondary outcome parameters of this study are: <br><br />• The (incremental) maximum amino acid concentration ((i)Cmax), (incremental) area under the concentration curve ((i)AUC) and t½ iAUC comparing all study products for total AA<br /><br>• Gastric emptying half time (t1/2), Cmax, and time until Cmax is reached (Tmax) and AUC (plasma concentrations of paracetamol) comparing all study products<br /><br>• Satiety questionnaire<br>