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CompletedNCT00799630Updated Dec 1, 2008

Effects of Nutraperf Consumption in Runners

An interventional study of Carbohydrate drink in Nutrition Processes, sponsored by Lescuyer Laboratory. Completed at 1 site in France. Open to male participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2008-12-01.

Sponsored by Lescuyer Laboratory · Not applicable and Interventional

Phase
Not applicable
Study type
Interventional
Enrollment
14
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
Male
01

Study summary

Exercise has numerous health benefits. Nevertheless, when exercise duration is \~45 min or longer and intensity moderate to intense, it may induce different troubles, for example: hypoglycemia, peripheral and central fatigue, muscle damages, osteoarticular injuries, inflammation, cardiovascular dysfunctions. Nutritional loading during exercise may prevent and and/or reduce some of these troubles.

In regard of recent data, we proposed a novel energy drink (NUTRAPERF®) to limit deleterious effects of long time exercise in neutral environment (outside temperature between 4 and 25°C) and to improve performance. If performance may be increased by this energy drink during long time exercise, we proposed that it consumption may also improve performance in short and sub-maximal exercise.

So, the purpose of this study is to investigate the effects of the consumption of this novel energy drink on performance during long and short time exercise. Moreover, we studied the effects of this consumption on different metabolic parameters (heart rate, oxygen consumption, respiratory quotient, ventilation, glycemia, lactatemia), on central and peripheral fatigue and on cognitive parameters.

02

Conditions studied

  • Nutrition Processes

Keywords

  • energy drink
  • exercise
  • BCAA
  • peripheral and central fatigue
03

In context

Lead sponsor

Lescuyer Laboratory is the lead sponsor of 8 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion criteria

  • Man aged between 18 and 45 years.
  • Regular sportsman (2 to 4 workouts by week since 3 months minimum).
  • Be a long-distance runner.
  • Be affiliated or beneficial to the National French Security Social.

Non-inclusion criteria

  • Any subject who was injured during the three preceding months study.
  • Any subject with a history of disease can disrupt the tests. In particular, subjects with pathological conditions placed on the joints of the knee or ankle (sprain repeated problems or patellar ligament) that could hamper measures of force maximum extension and flexion on these joints or illnesses that prevent the exercise of pedalling or running on treadmill (tendonitis, periostitis) will be excluded.
  • Any subject who at the same time participates at another medical experiment.
05

Study design

Phase
Not applicable
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
14 participants (actual)

Interventions

  • Dietary supplementCarbohydrate drink

    Maltodextrins, dextrose, fructose, amino acids (leucine, isoleucine, valine), natural flavors, sodium chloride, magnesium citrate, zinc, lactate, acid: malic acid, anti-caking agent: silicon dioxide; Curcumin (turmeric extract) , Thickener: xanthan gum, caffeine, vitamin C (Acerola extract), vitamin E - B1 - B2 - B3; piperine (black pepper extract).

    Also known as: NUTRAPERF

06

Study locations

1 site
  • Service de Physiologie Clinique et de l'Exercice, CHU Saint-Etienne
    Saint-Etienne, 42055, France
07

References and documents

Publications

  • Peltier SL, Vincent L, Millet GY, Sirvent P, Morin JB, Guerraz M, Geyssant A, Lescuyer JF, Feasson L, Messonnier L. Effects of carbohydrates-BCAAs-caffeine ingestion on performance and neuromuscular function during a 2-h treadmill run: a randomized, double-blind, cross-over placebo-controlled study. J Int Soc Sports Nutr. 2011 Dec 7;8:22. doi: 10.1186/1550-2783-8-22. PubMed 22152427 ↗
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 1, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00799630
Lead sponsor
Lescuyer Laboratory
Collaborators
Centre Hospitalier Universitaire de Saint Etienne, Université Savoie Mont Blanc
First posted
Dec 1, 2008
Start date
Nov 2008
Last update
Dec 1, 2008

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Nov 2008. You cannot join it, but the record below documents what was studied.

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