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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


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

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