Clinical Trials Directory

Trials / Completed

CompletedNCT03000582

Assessment of Different Forms of Creatine

Pharmacokinetic Assessment of Acute Ingestion of Different Forms of Creatine

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
13 (actual)
Sponsor
Texas A&M University · Academic / Other
Sex
Age
Healthy volunteers
Accepted

Summary

The purpose of this study is to examine the pharmacokinetics of creatine nitrate supplementation.

Detailed description

Creatine nitrate contains several nutrients that may increase anaerobic exercise performance. Theoretically, dietary supplementation of creatine nitrate during resistance training can improve the quality of training leading to greater changes in strength, power and fat free mass. Endothelial function measured by flow-mediated dilation (FMD), a non-invasive vascular health parameter that can be measured via ultrasonography, is a predictor of cardiovascular disease risk which precedes traditional risk markers. Diet, physical activity and pharmaceutical interventions can all impact vascular function and health. The purpose of this study is to determine the acute vascular response of creatine nitrate supplementation on FMD by analyzing the pharmacokinetics of creatine nitrate supplementation.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTCreatine monohydrateCreatine monohydrate (5.0 g creatine monohydrate, 1.5 g dextrose)
DIETARY_SUPPLEMENTCreatine nitrate-1Creatine nitrate-1 (1.0 g creatine monohydrate, 0.5 g nitrate, 5.0 g dextrose)
DIETARY_SUPPLEMENTCreatine nitrate-2Creatine nitrate-2 (2.0 g creatine monohydrate, 1.0 g nitrate, 3.5 g dextrose)
DIETARY_SUPPLEMENTPlaceboPlacebo (6.5 g dextrose)

Timeline

Start date
2014-06-01
Primary completion
2014-09-01
Completion
2014-09-01
First posted
2016-12-22
Last updated
2016-12-22

Source: ClinicalTrials.gov record NCT03000582. Inclusion in this directory is not an endorsement.