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The Effect of Probiotic Intervention on Intestinal Permeability

NCT03027583 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 251

Last updated 2018-05-03

No results posted yet for this study

Summary

This trial is a single-site, randomised, double blind, placebo-controlled, two-armed parallel-group trial in healthy adult volunteers. The trial will investigate the effect of oral supplementation of a probiotic strain on the ability to attenuate exercise-induced deterioration of intestinal barrier function and gastrointestinal symptoms.

Conditions

  • Intestinal Permeability

Interventions

DIETARY_SUPPLEMENT

Probiotic

6 weeks daily oral intake of a probiotic strain.

DIETARY_SUPPLEMENT

Placebo

6 weeks daily oral intake of placebo.

Sponsors & Collaborators

  • Atlantia Food Clinical Trials

    collaborator INDUSTRY

  • Signifikans ApS

    collaborator OTHER

  • Chr Hansen

    lead INDUSTRY

Principal Investigators

  • Fergus Shanahan, Professor · Cork University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-03-01
Primary Completion
2017-07-30
Completion
2017-09-15

Countries

  • Ireland

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 NCT03027583 on ClinicalTrials.gov