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Medium Chain Triglycerides Plasma Profile and Their Metabolites After Oral Peptamen Intake

N

Nestlé

Status

Completed

Conditions

Healthy

Treatments

Dietary Supplement: Peptamen 1.5

Study type

Interventional

Funder types

Industry

Identifiers

NCT02241681
14.22.MET

Details and patient eligibility

About

Medium Chain Triglycerides (MCT) have been used for many years as a good source of lipid to decrease potential for fat malabsorption. However, the pharmacokinetics of MCT and of their metabolites have not been explored in details.

This is an exploratory study aiming at determining the plasma level of MCT and their metabolites after oral intake of Peptamen.

Full description

20 subjects will be given 250mL of peptamen 1.5 twice, with 4 hours of interval, on a single day.

Plasma kinetics of MCTs and their metabolites will be made over 8 hours from baseline

Enrollment

20 patients

Sex

All

Ages

20 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy males and females
  • Aged between 20 and 65 years old
  • BMI in the normal range (18.5 to 25.0 kg/m2)
  • Having signed his/her consent form

Exclusion criteria

  • Clinically relevant digestive (including malabsorption or major surgery), renal, hepatic, pancreatic or metabolic disease (diabetes, hypo or hyperthyroidism, hypo or hypercorticism), as determined by the medical (screening) visit and a standard blood chemistry analysis (glucose, total cholesterol, ALDL, AHDL, triglycerides, ASAT, ALTI, gamma GT, RCRP, creatinine)
  • Medically diagnosed anemia based on a blood formula
  • Food allergy, lactose intolerance and intolerance to milk proteins (anamnesis)
  • Smokers (anamnesis)
  • Pregnancy (anamnesis)
  • Under corticoids or hormone (adrenal, thyroid) treatment
  • Alcohol intake: > 2 units a day (anamnesis)
  • Consumption of illicit drugs (anamnesis)
  • Having given blood within the last month, or willing to make a blood donation until one month following the end of the study
  • Subject who cannot be expected to comply with the study procedures, including consuming the test product
  • Currently participating or having participated in another clinical trial during the last month prior to the beginning of this study.

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Peptamen 1.5
Other group
Description:
500 mL of Peptamen 1.5
Treatment:
Dietary Supplement: Peptamen 1.5

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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