Bioavailability, Pharmacokinetic and Mechanistic Study of Sinetrol® Xpur, a Polyphenol-rich Ingredient
NCT03823196 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2019-11-01
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
- DIETARY_SUPPLEMENT
-
Verum900
Sinetrol® 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_SUPPLEMENT
-
Verum1800
Sinetrol® 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
Sponsors & Collaborators
-
Fytexia
lead INDUSTRY
Principal Investigators
-
Pedro E Alcaraz Ramon · UCAM
Study Design
- Allocation
- RANDOMIZED
- Purpose
- BASIC_SCIENCE
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 20 Years
- Max Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2019-03-08
- Primary Completion
- 2019-07-31
- Completion
- 2019-10-31
Countries
- Spain
Study Locations
More Related Trials
-
A Trial of SHR6390 in Healthy Caucasian Volunteers
NCT04301804 ·Status: COMPLETED ·Phase: PHASE1
-
A Pharmacokinetic Study of VCT220 in Particicants With Hepatic Injury and Normal Hepatic Function
NCT06938529 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetic Study of Stiripentol and Its Metabolites After Multiple Dose Oral Administration in Healthy Male Volunteers
NCT03866928 ·Status: COMPLETED ·Phase: PHASE1
-
Phase 1 PK Study to Evaluate the PK of CIN-107 in Subjects With Hepatic Impairment
NCT05961397 ·Status: COMPLETED ·Phase: PHASE1
-
Study to Evaluate Orelabrutinib Tablets in Subjects With Hepatic Impairment and Healthy Subject
NCT05684653 ·Status: UNKNOWN ·Phase: PHASE1
-
Study to Investigate Relative Bioavailability of Different Formulations of SHR6390 in Healthy Subjects
NCT04667156 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Examine the Absorption of GSK561679 in Healthy Male Volunteers
NCT00539136 ·Status: COMPLETED ·Phase: PHASE1
-
A Trial to Study the Absorption, Metabolism, and Excretion of [14C]-Olinciguat in Healthy Male Volunteers
NCT03795519 ·Status: COMPLETED ·Phase: PHASE1
-
A Pharmacokinetics and Tolerability Study of Fedratinib in Subjects With Moderate and Severe Hepatic Impairment
NCT03983161 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetics, Safety, and Tolerability of Methylnaltrexone in Volunteers With Impaired Hepatic Function
NCT01367522 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetic Study of ABT-126 in Healthy Volunteers
NCT00959634 ·Status: COMPLETED ·Phase: PHASE1
-
A Study Evaluating the Pharmacokinetics of Three QRL-101 Formulations in Healthy Participants
NCT06877624 ·Status: COMPLETED ·Phase: PHASE1
-
Open-Label Pharmacokinetic Study of Final Formulations of ATX-101
NCT01632917 ·Status: COMPLETED ·Phase: PHASE1
-
Open Label Study Evaluating the Effects of a Single Oritavancin Infusion on Cytochrome P450 in Healthy Volunteers
NCT01784536 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Assess the Pharmacokinetics and Food Effect of SR419 in Healthy Subjects
NCT04705077 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetics of Mitiperstat in Participants With Hepatic Impairment
NCT05751759 ·Status: COMPLETED ·Phase: PHASE1
-
Mass Balance and Pharmacokinetics of [14C]-CRN00808 in Healthy Volunteers
NCT04246749 ·Status: COMPLETED ·Phase: PHASE1
-
Effect of Itraconazole on the Pharmacokinetics of Bardoxolone Methyl in Healthy Adults
NCT03264079 ·Status: COMPLETED ·Phase: PHASE1
-
An Explorative Study on the Pharmacokinetics and Pharmacodynamics of Sunitinib in Healthy Volunteers
NCT00904657 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Investigate the Effect of Hepatic Impairment on the Pharmacokinetics of a Single Dose of Cenerimod
NCT04819464 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of the Absorption, Metabolism, and Excretion of [14C]-AMG 510 Following a Single Oral Dose in Healthy Male Subjects
NCT05578859 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetic Study to Characterize Phenotyping Metrics of the "Basel" Cocktail After CYP Induction or Inhibition
NCT01386593 ·Status: COMPLETED ·Phase: PHASE1
-
Study to Investigate the Tolerability, Safety, Pharmacokinetics, and Pharmacodynamics of ACT-389949
NCT02099071 ·Status: COMPLETED ·Phase: PHASE1
-
Absorption, Metabolism, Excretion and Absolute Bioavailability
NCT03250039 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of the Absorption, Metabolism and Excretion of [14C]XZP-3621 in Human
NCT05836805 ·Status: UNKNOWN ·Phase: PHASE1