Clinical Trials Directory

Trials / Completed

CompletedNCT06062511

Poplar-type Propolis Dry Extract ESIT12 : Nutrikinetic and Bioavailability Studies

Evaluation of Nutrikinetic and Bioavailability of Phenolic Compounds From ESIT12, a Poplar-type Propolis Dry Extract

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Fytexia · Industry
Sex
All
Age
25 Years – 69 Years
Healthy volunteers
Accepted

Summary

The aim of this study is to investigate phenolic compounds from ESIT12, a poplar-type propolis ingredient, bioavailability and nutrikinetics by measuring urinary excretion and metabolic profile over 48h by means of high-performance liquid chromatography coupled with tandem mass spectrometry (HPLC-MS/MS). The study follows a cross-over, double-blind, randomized and placebo control design on 10 healthy subjects.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTESIT12 DESIT12 is a poplar-type propolis powder extract containing phenolic compounds from flavonoids and phenolic acids family. ESIT12 D contains 400 mg of ESIT12
DIETARY_SUPPLEMENTESIT12 4DESIT12 is a poplar-type propolis powder extract containing phenolic compounds from flavonoids and phenolic acids family. ESIT12 4D contains 1600 mg of ESIT12
DIETARY_SUPPLEMENTPlaceboPlacebo is composed of the carriers of ESIT12 : arabic gum, sucrose and silicon dioxide mix

Timeline

Start date
2023-07-22
Primary completion
2023-10-10
Completion
2023-10-10
First posted
2023-10-02
Last updated
2023-12-08

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT06062511. Inclusion in this directory is not an endorsement.