Effects of Nitrates and Citrulline Malate on Performance in Professional Professional Soccer
NCT ID: NCT05525871
Last Updated: 2023-11-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
40 participants
INTERVENTIONAL
2022-08-15
2023-01-20
Brief Summary
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Detailed Description
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The product to be consumed will be Nitrates and Citrulline Malate. Participants will consume the product for 30 days. The intake should be done two hours before each training session and the same dose will be consumed.
The women's soccer players will perform a stress test with gas analysis to measure performance, as well as a Wingate test without consumption of the products. Five days later, the players will perform the Yo-Yo IR1 test in the field and will repeat the same tests performed at the beginning of the test after product consumption.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
QUADRUPLE
Study Groups
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Nitrates and Citrulline Malate
Gel elaborated from fruit puree with high polyphenol content, with the addition of nitrates and citrulline malate as study supplements. addition of nitrates and citrulline malate as study supplements.
Nitrates and Citrulline Malate
Female soccer players should consume the experimental product for 30 days to evaluate the efficacy of a sports supplement high in nitrates combined with citrulline malate in the improvement of performance in high-intensity intermittent exercise.
high intensity
Control product
Consumption of placebo product (Fruit puree)
Control product
Fruit puree
Interventions
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Nitrates and Citrulline Malate
Female soccer players should consume the experimental product for 30 days to evaluate the efficacy of a sports supplement high in nitrates combined with citrulline malate in the improvement of performance in high-intensity intermittent exercise.
high intensity
Control product
Fruit puree
Eligibility Criteria
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Inclusion Criteria
* Female.
* Healthy subjects without any chronic disease.
* Volunteers capable of understanding the clinical study, willing to give their written informed. consent and comply with the procedures and requirements of the study. and requirements of the study.
Exclusion Criteria
* Smoking subjects.
* Subjects using mouthwashes during the study.
* Subjects with a history of drug, alcohol or other substance abuse or other factors that limit their ability to cooperate during the study. factors that limit their ability to cooperate during the study.
* Subjects whose status makes them ineligible for the study, at the discretion of the investigator discretion of the investigator.
18 Years
40 Years
FEMALE
Yes
Sponsors
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Universidad Católica San Antonio de Murcia
OTHER
Responsible Party
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Francisco Javier López Román
Principal Investigator
Locations
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Catholic University of Murcia
Murcia, , Spain
Countries
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Other Identifiers
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UCAMCFE-00027
Identifier Type: -
Identifier Source: org_study_id