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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01353872
Other study ID # 2010-A00724-35
Secondary ID
Status Completed
Phase N/A
First received May 13, 2011
Last updated May 13, 2011
Start date October 2010
Est. completion date May 2011

Study information

Verified date May 2011
Source Lescuyer Laboratory
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)France: Committee for the Protection of Personnes
Study type Interventional

Clinical Trial Summary

The main objective of this study is to investigate the effects of ingestion of different sports drinks (Nutrattente / Nutraperf / Nutrarecup) on fatigue induced by a tennis tournament simulation.


Recruitment information / eligibility

Status Completed
Enrollment 8
Est. completion date May 2011
Est. primary completion date May 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria:

- About 18 to 35 years (inclusive) Subject has a stable weight for at least three months before the start of the study

- Subject able and willing to comply with the protocol and agreeing to give their consent in writing

- Subject affiliated with a social security scheme

- Subject willing to be included in the national register of volunteers who lend themselves to biomedical research

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator)


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Nutrattente / Nutraperf / Nutrarecup
500 mL of Nutrattente before each match 500 mL/h of Nutraperf during each match 250 mL of Nutrarecup after each match
Nutrattente placebo / Nutraperf placebo / Nutrarecup placebo
500 mL of Nutrattente placebo before each match 500 mL/h of Nutraperf placebo during each match 250 mL of Nutrarecup placebo after each match

Locations

Country Name City State
France Sirvent Aubiere

Sponsors (3)

Lead Sponsor Collaborator
Lescuyer Laboratory Service de Médecine du Sport et des Explorations Fonctionnelles - CHU G Montpied - Clermont-Ferrand, Université Blaise Pascal, Clermont-Ferrand

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary peripheral fatigue measured by surface electromyographic (EMG) signal from the right triceps muscle 3 matches (1.5 days) No
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