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The Antioxidant Efficacy of a Product Probiotic in Research

NCT03798821 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2019-01-10

No results posted yet for this study

Summary

Determine the efficacy of the investigational product versus placebo in reducing stress oxidative during the performance of a physical exercise of a certain intensity and duration.

Conditions

  • Oxidative Stress

Interventions

DIETARY_SUPPLEMENT

Lactobacillus rhamnosus, Lactobacillus casei y Bifidobacterium longum (100MG)

six weeks of consumption

DIETARY_SUPPLEMENT

Lactobacillus rhamnosus, Lactobacillus casei y Bifidobacterium longum (300MG)

six weeks of consumption

DIETARY_SUPPLEMENT

maltodextrin and sucrose (PLACEBO)

six weeks of consumption

Sponsors & Collaborators

  • Universidad Católica San Antonio de Murcia

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-01-08
Primary Completion
2018-07-30
Completion
2019-01-04

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03798821 on ClinicalTrials.gov