Viewing Study NCT03288623



Ignite Creation Date: 2024-05-06 @ 10:32 AM
Last Modification Date: 2024-10-26 @ 12:32 PM
Study NCT ID: NCT03288623
Status: COMPLETED
Last Update Posted: 2019-04-17
First Post: 2017-09-14

Brief Title: The Effects of Dark Chocolate Implementation in Elite Athletes
Sponsor: University of Roma La Sapienza
Organization: University of Roma La Sapienza

Study Overview

Official Title: The Effects of Dark Chocolate Implementation in the Reduction of Oxidative Stress and Improvement of Vascular Function and Physical Performance in Elite Athletes
Status: COMPLETED
Status Verified Date: 2019-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Dark chocolate DC is rich in epicatechin which augments nitric oxide NO production through endothelium-dependent influences The increased bioavailability and activity of NO have been demonstrated to statistically increase flow-mediated dilation in healthy subjects and in hypertensive patients DC supplementation has been hailed for its positive effects on cardiovascular health and it has been proposed as a booster of physical performance in athletes however the mechanisms by which DC improves oxidative stress vascular function and athletic performance are not fully understood The investigators designed a human study assessing how DC improves NO bioavailability and activity in elite athletes Twenty-four elite soccer players aged 18-35 years old all males are divided in 2 groups and randomly assigned to receive DC 85 cocoa 40g per day or whitemilk chocolate 35 cocoa for 30 days The primary outcome measure is the evaluation of Soluble NOX2-derived peptide sNOX2-dp a direct marker of NADPH oxidase activation The secondary outcome measures are other markers of oxidative stress as the soluble P-selectin sPs Vitamin E soluble CD40 Ligand sCD40L a marker of in vivo platelet activation and flow-mediated dilation assessed by vascular ultrasound All parameters are assessed at baseline and after 30 days in both groups
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None