Clinical Trials Directory

Trials / Completed

CompletedNCT04506385

Metabolomic Effects of Probiotics Administration

Effects of Probiotics Administration on Human Metabolic Phenotype

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
42 (actual)
Sponsor
Probiotical S.p.A. · Industry
Sex
All
Age
24 Years – 65 Years
Healthy volunteers
Accepted

Summary

Background: The establishment of the beneficial interactions between the host and its microbiota is essential for the development and correct functioning of the organism, since microflora alterations can lead to many chronic degenerative diseases. In this context, probiotics are used to improve balanced microbial communities and therefore exert substantial health-promoting effects to the host. Objective: The aim of the present study is to monitor the molecular outcomes, obtained by gut microflora modulation through probiotic treatment, on human urine and serum metabolic profiles, with a 1H-Nuclear Magnetic Resonance -based metabolomic approach.

Detailed description

Design: In a first phase twenty-two healthy subjects are enrolled in the study and administered with Lactobacillus delbrueckii subs. delbrueckii and/or a mix of 5 biotypes of Bifidobacterium longum for 8 weeks. In the second phase subjects are enrolled in the study and administered with Lactobacillus rhamnosus, Lactobacillus plantarum, Lactobacillus fermentum and Bifidobacterium longum at two different concentration. During the course of the study all the probiotic types were administered both singularly and in combination. From each subject urine and serum samples are collected before and during the supplementation and are analysed by nuclear magnetic resonance spectroscopy and statistical analyses.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTprobioticsIn the first phase: 10 subjects have added in the diet a daily dose of 1 billion of freeze-dried LDD01 probiotics (A arm), 12 individuals are supplemented with a daily dose of 1 billion of the DLBL mix (B arm). In the second phase: 10 individuals are supplemented with a daily low dose of probiotics blend (C arm) and 10 individuals are supplemented with a daily high dose of probiotics blend (D arm).

Timeline

Start date
2020-04-20
Primary completion
2020-07-31
Completion
2021-03-31
First posted
2020-08-10
Last updated
2023-01-25

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT04506385. Inclusion in this directory is not an endorsement.