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Effects of an Amino-acid Supplement on Hepatic Lipid Metabolism (AMINOFRUCT)

U

University of Lausanne (UNIL)

Status

Completed

Conditions

Metabolic Syndrome

Treatments

Dietary Supplement: Fructose+maltodextrin placebo
Dietary Supplement: amino-acid + fructose

Study type

Interventional

Funder types

Other

Identifiers

NCT01119989
protocole 51/10

Details and patient eligibility

About

10 healthy male volunteers will be studied after

  • a 6 day weight maintenance, balanced diet
  • a 6 days weight maintenance, balanced diet supplemented with 3 grams fructose/kg body weight/day
  • a 6 days weight maintenance, balanced diet supplemented with 3 grams fructose/kg body weight/day and 20g amino-acids per day At the end of each 6 days period, the following measurements will be obtained
  • intrahepatic lipids (1H-MRS)
  • metabolic effects of fructose ingestion (measurement of substrate oxidation, gluconeogenesis from fructose, palmitate synthesis from fructose, plasma VLDL-kinetics)

This is a randomized, double blinded study

Enrollment

9 patients

Sex

Male

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • age 18-30 years
  • sex: males
  • BMI between 19 and 25 kg/m2
  • less than 3 30min- exercise session/week

Exclusion criteria

  • smokers
  • alcohol consumption more than 50g/week
  • consumption of drugs
  • history of diabetes in first degree relatives
  • presence of ferro-magnetic prosthesis, cardiac pacemakers, or any contra-indication to NMR

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Triple Blind

9 participants in 3 patient groups, including a placebo group

weight maintenance diet
No Intervention group
weight maintenance + fructose
Placebo Comparator group
Treatment:
Dietary Supplement: Fructose+maltodextrin placebo
weight maintenance diet + fructose and amino-acid
Experimental group
Treatment:
Dietary Supplement: amino-acid + fructose

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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