Clinical Trials Directory

Trials / Completed

CompletedNCT03823196

Bioavailability, Pharmacokinetic and Mechanistic Study of Sinetrol® Xpur, a Polyphenol-rich Ingredient

Bioavailability, Pharmacokinetic and Mechanistic Study of Sinetrol® Xpur, a Polyphenol-rich Ingredient: an Open-label Study on Overweight Volunteers During a Chronical Supplementation and a Post-supplementation Follow-up

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Fytexia · Industry
Sex
All
Age
20 Years – 50 Years
Healthy volunteers
Accepted

Summary

The purpose of the study is to investigate the metabolization and the bioavailability of bioactive compounds from Sinetrol® Xpur, a polyphenol-rich ingredient, during a 16-week long chronical supplementation. It will be investigated the mechanism of action in adipocyte cells to try to explain the beneficial effects of the ingredient on body composition, especially on both abdominal subcutaneous and visceral fat mass.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTVerum900Sinetrol® Xpur is a blend of polyphenol-rich extracts from grapefruit, guarana seed, sweet orange and blood orange. Daily dosage is 900 mg for 16 weeks
DIETARY_SUPPLEMENTVerum1800Sinetrol® Xpur is a blend of polyphenol-rich extracts from grapefruit, guarana seed, sweet orange and blood orange. Daily dosage is 1800 mg for 16 weeks

Timeline

Start date
2019-03-08
Primary completion
2019-07-31
Completion
2019-10-31
First posted
2019-01-30
Last updated
2019-11-01

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT03823196. Inclusion in this directory is not an endorsement.