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OpenTrials
Completed

NCT Number: NCT01128647

Disposal of Oral Fructose During Exercise

There is evidence that total carbohydrate oxidation during exercise is higher after ingestion of fructose:glucose mixture than after ingestion of equimolar amounts of glucose alone. This may possible contribute to improve performance, provided that the extra carbohydrate oxidation induced by fructose:glucose co-ingestion occurs in skeletal muscle. The present study aims at assessing the hypothesis that, during exercise, a substantial portion of oral fructose is converted into lactate prior to oxidation To identify the major pathways of fructose disposal, 7 healthy endurance trained male volunteers will be studied. For each participant the following measurement will be performed

* a measurement of maximal oxygen consumption (VO2 max) on an ergometric bicycle * a 2 hour exercise protocol with oral administration of a glucose drink. 6,6-2H2 glucose (0.44 µmol/kg/min) and 13C3 lactate (2.25 µmol/kg/min) will be infused to calculate glucose and lactate kinetics. Indirect calorimetry will be performed to measure total carbohydrate oxidation and expired 13CO2 will be monitored to calculate whole body lactate oxidation * a 2 hour exercise protocol with oral administration of a glucose:fructose (72 + 48 g every hour) mixture. 6,6-2H2 glucose (0.44 µmol/kg/min) and 13C3 lactate (2.25 µmol/kg/min) will be infused to calculate glucose and lactate kinetics. Indirect calorimetry will be performed to measure total carbohydrate oxidation and expired 13CO2 will be monitored to calculate whole body lactate oxidation * a 2 hour exercise protocol with oral administration of a glucose:fructose (72 + 48 g every hour) mixture with fructose labelled with 13C6 fructose to evaluate exogenous fructose metabolic fate and oxidation. 6,6-2H2 glucose (0.44 µmol/kg/min) will be infused to calculate glucose kinetics. Fructose conversion into lactate and glucose will be evaluated by monitoring the systemic appearance of plasma 13C-labelled lactate and 13C-labelled glucose. Total exogenous fructose oxidation will be measured by monitoring 13CO2 production.

Based on these measurements, semi-quantitative estimates of total fructose oxidation, fructose conversion into glucose, fructose conversion into lactate, and oxidation of fructose-derived lactate will be obtained

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Key information

Age range

18 year–35 year

Sex eligibility

Male

Study type

Observational

Primary location

Centre Hospitalier Universitaire Vaudois

Lausanne, CH-1011, Switzerland

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age between 18 and 35 years
  • males
  • good physical health
  • weekly cycling training sessions (> 3 sessions/week)

Exclusion criteria

  • diabetes or glucose intolerance
  • past history of heart disease
  • alcohol intake > 30 g/day
  • smokers
  • drug consumption

Treatment and study plan

Fructose:glucose drink

Dietary Supplement

glucose drink

Dietary Supplement

Primary outcomes

  1. Fructose conversion into lactate

    Time frame: during a 2 hour-exercise at 60% VO2 max

Secondary outcomes

  1. Total exogenous fructose oxidation

    Time frame: during a 2 hour-exercise at 60% VO2 max

  2. Fructose conversion into glucose

    Time frame: during a 2 hour-exercise at 60% VO2 max

  3. Oxidation of lactate derived from fructose

    Time frame: during a 2 hour-exercise at 60% VO2 max

Sponsors and collaborators

Lead sponsor

University of Lausanne

Other

Registry information

Important dates

Study start
2009
Primary completion
2009
Study completion
2010
First posted
May 24, 2010
Registry last updated
Feb 13, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.