Effect of Probiotics on the Intestinal Microbiota of Pediatric Patients

Status Not yet recruiting

Clinical Trial Summary

Numerous studies have described an altered gut microbiota composition (dysbiosis) in patients with neurodevelopmental disorders that can be correlated with their symptoms, especially gastrointestinal symptoms. An interventional, randomised, double-blind, placebo-controlled study will be conducted to investigate the effect of a probiotic supplement on the microbiota composition of children aged 3-7 years with neurodevelopmental issues. The duration of the study will be of 6 months approximately, including 6 months of product intake. Participants will be randomly assigned to one of the two study groups: control group with placebo administration or probiotic administration group.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Neurodevelopmental Disorders

Clinical Trial Details

NCT number	NCT06352203
Study type	Interventional
Source	ProbiSearch SL
Contact	Susana Manzano Jiménez, PhD
Phone	+34 918035179
Email	susana.manzano@probisearch.com
Status	Not yet recruiting
Phase	N/A
Start date	April 2024
Completion date	November 2025

View Details

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