RecruitingNot ApplicableNCT06514573

Butyrate Supplementation in Children With Autism Spectrum Disorder (ASD) and Functional Gastrointestinal Disorders

Effects of a Postbiotic Supplementation on Gastrointestinal and Core Symptoms in Autism Spectrum Disorder: A Multicenter Randomized Controlled Trial


Sponsor

Istituto Superiore di Sanità

Enrollment

128 participants

Start Date

May 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Autism spectrum disorder (ASD) is a neurodevelopmental condition occurring in 1:77 Italian children. Several comorbidities are reported, including functional gastrointestinal disorders (FGIDs) present in up to 70% of patients. FGIDs are disorders resulting from a combination of symptoms affecting motility, hypersensitivity, and other functions, which are not caused by anatomic or organic origin and that impact the severity of ASD core symptoms and complicate the clinical management of ASD children, especially those who are non-verbal. Evidence reports gut microbiome (GM) remodelling in ASD children, and postbiotic butyrate, a GM-derived metabolite, attenuates FGIDs in children and restores social behavior in ASD mouse models. Clinical data on butyrate effects in ASD are still scanty. The present study investigates the therapeutic effects of a 16-week oral postbiotic supplementation on clinical/behavioral profiles, gastrointestinal disturbances, gut microbiome, and immune and inflammatory biomarkers in peripheral blood and fecal samples in children with ASD and FGIDs. Using the Machine Learning (ML) approach, a subset of artificial intelligence, this study also aims to identify predictive factors implicated in the effect of the postbiotic supplementation on FGIDs, important for prevention through modulation of the microbiota. The investigators expect that treating FGIDs will have an impact on the behavioral and core symptoms of ASD and the quality of life of children and their families.


Eligibility

Min Age: 3 YearsMax Age: 6 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Placebo (cornstarch) and Sodium Butyrate for people with autism spectrum disorder (asd). The study is currently recruiting participants at 3 locations. People eligible for this study include aged 3 Years to 6 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIETARY_SUPPLEMENTSodium Butyrate

Daily supplementation with 1 sachet per day for 16 weeks

DIETARY_SUPPLEMENTPlacebo (cornstarch)

Daily supplementation with 1 sachet per day for 16 weeks


Locations(3)

Azienda Ospedaliera Universitaria Federico II

Naples, Italy

Policlinico Tor Vergata Hospital

Rome, Italy

Istituto Superiore di Sanità

Rome, Italy

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NCT06514573


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