NCT02717234
Completed
Not Applicable
Appearance of Plasma Amino Acids Following Consumption of an Oral Nutrition Supplement
Société des Produits Nestlé (SPN)0 sites12 target enrollmentFebruary 2016
ConditionsHealthy Subjects
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Healthy Subjects
- Sponsor
- Société des Produits Nestlé (SPN)
- Enrollment
- 12
- Primary Endpoint
- Change in plasma arginine levels in µmol/L
- Status
- Completed
- Last Updated
- 3 years ago
Overview
Brief Summary
To assess the effect of consumption of an oral nutrition supplement on Arginine, a blood marker of nutritional intake
Investigators
Eligibility Criteria
Inclusion Criteria
- •Healthy subject (absence of metabolic disorder, heart disease, endocrine disease, cancer)
- •Discontinued use of omega 3 fatty acid supplements - 10 days prior to testing
- •Willing to provide signed informed consent
Exclusion Criteria
- •Patients with potential for non-compliance
- •Patients with allergy to ingredients in test products (i.e. milk protein, fish oil)
- •Subject who in the Investigator's assessment cannot be expected to comply with study protocol
- •Currently participating in another conflicting clinical trial.
Outcomes
Primary Outcomes
Change in plasma arginine levels in µmol/L
Time Frame: Pre-consumption, 30, 60, 120, 180, 240 minutes
Secondary Outcomes
- Change in plasma phospholipid Eicosapentaenoic acid (EPA) in µg/ml(Pre-consumption, 30, 60, 120, 180, 240 minutes)
- Change in plasma-free phospholipid Eicosapentaenoic acid (EPA) in µg/ml(Pre-consumption, 30, 60, 120, 180, 240 minutes)
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