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Clinical Trials/NCT02717234
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

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

Registry
clinicaltrials.gov
Start Date
February 2016
End Date
May 2016
Last Updated
3 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Société des Produits Nestlé (SPN)
Responsible Party
Sponsor

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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