Clinical Trials Directory

Trials / Unknown

UnknownNCT03523936

Gut Microbiota and Antibiotics - Prevention of Side Effects by New Prebiotics

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Turku University Hospital · Other Government
Sex
All
Age
2 Years – 6 Years
Healthy volunteers
Not accepted

Summary

Antibiotics disturb the balance of gut microbiota causing dysbiosis. The purpose of this double-blind placebo controlled intervention study is to investigate whether a new prebiotic product could prevent the side effects of antibiotics.

Detailed description

Thirty children (2-6 years of age), who require antibiotic treatment assessed by a doctor, will be enrolled in the study. The children will be randomized to receive either the prebiotic product or placebo during the course of antibiotic treatment. The children will give a faecal sample in the beginning and at the end of the study. The samples will be used for the analysis of microbiota and differences in the microbiota between the groups.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTPrebiotic productPrebiotic product used during the course of antibiotic treatment
DIETARY_SUPPLEMENTPlaceboPlacebo

Timeline

Start date
2018-06-01
Primary completion
2019-12-31
Completion
2019-12-31
First posted
2018-05-14
Last updated
2018-05-14

Source: ClinicalTrials.gov record NCT03523936. Inclusion in this directory is not an endorsement.