Pure Global

Creatine Supplementation for Female Football - Trial NCT06250556

Access comprehensive clinical trial information for NCT06250556 through Pure Global AI's free database. This phase not specified trial is sponsored by University of Sao Paulo and is currently Recruiting. The study focuses on Athletes. Target enrollment is 70 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

Free Database
Powered by Pure Global AI
840K+ Trials
NCT06250556
Recruiting
dietary supplement
Trial Details
ClinicalTrials.gov โ€ข NCT06250556
View on ClinicalTrials.gov
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Creatine Supplementation for Female Football
Creatine Supplementation in Young and Elite Female Football Players

Study Focus

Athletes

creatine

Interventional

dietary supplement

Sponsor & Location

University of Sao Paulo

Sรฃo Paulo,Sao Paulo, Brazil

Timeline & Enrollment

N/A

Feb 10, 2024

Dec 30, 2024

70 participants

Primary Outcome

kidney function

Summary

Creatine is an effective, inexpensive, and safe dietary supplement, which has been largely
 used in sports and clinical populations. However, creatine is much less studied in female
 athletes, with long-term data being particularly scant. This study aims to expand our
 knowledge on the effects of creatine supplementation in young (Under-20) and elite female
 football players. This study will comprise two experiments. The first one will be a
 randomized, controlled trial in which young athletes will be assigned into either creatine or
 placebo (n = 20). Before and 7 days after supplementation or placebo (4 x 5 g/d of Creapure
 or dextrose at same dose), athletes will perform a battery of performance tests. Blood and
 urinary biochemical parameters for assessing the safety of supplementation will be analyzed
 (creatinine, albuminuria, urea, sodium, potassium, liver enzymes, creatine kinase,
 hematology). Food intake will be assessed by means of 3-d 24-h dietary recalls. The second
 experiment will have a quasi-experimental design (i.e., pre-to-post), in which both young and
 elite football players (n = 70) will be supplemented with creatine (4 x 5 g/d for 7 days and
 then 5 days during the follow-up) and will be assessed for safety using the above-mentioned
 markers during the regular football season (~12 months). Assessments will be carried out at
 baseline, in the mid-season and after the season.

ICD-10 Classifications

Examination for participation in sport
Striking against or struck by sports equipment
Routine general health check-up of sports teams

Data Source

ClinicalTrials.gov

NCT06250556

Non-Device Trial