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NCT Number: NCT07345585

Probiotics for Autism Spectrum Disorders: a Randomized Controlled Trial (The PASD Study)

Autism spectrum disorders (ASD) are a group of severe neurodevelopmental conditions characterized by impaired communication and social interaction, as well as repetitive/stereotyped behaviors deriving from a combination of genetic and environmental factors. The ASD diagnosis rates increased dramatically over the past number of decades. The Diagnostic and Statistical Manual of Mental Disorders (DSM-5) describes a worldwide prevalence of approximately 1%. The prevalence of ASD is 1 in 59 individuals in the US reported by the Centers for Disease Control and Prevention. According to the latest data from the Italian National Observatory for ASD, the actual prevalence in Italy is about 1/77 for children aged between 7 and 9 years, with a 4.4 times higher prevalence in male. The origin of ASD is still largely undefined. It has been hypothesized a possible role for the influence of early life alteration of gut microbiome (GM). We demonstrated an imbalance in Bacteroidetes and Firmicutes phyla with a decrease in Bacteroidetes/Firmicutes ratio in the GM of pediatric patients affected by ASD. Similar data have been observed by others. Data from ASD animal model confirm the presence of GM dysbiosis with significant correlation with behavioral, gastrointestinal and immunologic alterations. Altogether these data support the hypothesis that GM dysbiosis could be involved in the ASD pathogenesis. The ASD children present an increased prevalence of functional gastrointestinal disorders (FGIDs), mainly chronic constipation, functional diarrhea, and irritable bowel syndrome (IBS). A role for GM has been suggested also for these conditions. The presence of these disorders negatively influence the disease severity and the parental quality of life of ASD children. Starting from all these considerations GM is becoming a possible target of intervention for pediatric ASD. Probiotics are one of the most investigated strategy for a beneficial modulation of GM. Probiotics are commonly defined as live microorganisms which when ingested in adequate amounts confer a beneficial effect on the host. The most used probiotics in the pediatric age are Saccharomyces and Lactobacillus strains including Lactobacillus rhamnosus GG (LGG). Data report a beneficial influence elicited by LGG on GM structure and function. This probiotic resulted also effective in treating FGIDs patients. Preliminary evidence suggest the potential efficacy of probiotics for FGIDs treatment in ASD children. Altogether these evidence strongly support the hypothesis that LGG could exert a beneficial action in ASD children. The purpose of this study is to evaluate the therapeutic efficacy of LGG on FGIDs in ASD children.

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Key information

Age range

4 year–12 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Traslational Medical Science - University of Naples Federico II

Naples, 80131, Italy

Location status: Recruiting

Location contact

Roberto Berni Canani, MD, PhD

CONTACT

[email protected]

0817462680

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • children aged 4-12 years
  • children of both sex
  • children with a sure diagnosis of ASD and presence of FGIDs with a GSI ≥7 from at least 3 months.

Exclusion criteria

  • children aged <4 or >12 years
  • uncertain ASD and/or FGIDs diagnosis
  • FGIDs duration lasting <3 months
  • concomitant presence of other chronic conditions (adverse food reactions; genetic and metabolic disorders; malformations of GI, respiratory or urinary tract; neurologic diseases; immunodeficiencies; diabetes; cardiovascular diseases; autoimmune diseases; chronic infections; chronic respiratory, GI or urinary tract diseases; obesity; tumors; malnutrition).
  • use of antibiotics and/or pre-/pro-/ synbiotics during the 6 months prior to enrolment
  • participation into other clinical trials during the last 12 months.

Treatment and study plan

Lactobacillus rhamnosus GG

Other

Lactobacillus rhamnosus GG

Placebo

Other

Placebo

Primary outcomes

  1. Functional gastrointestinal disorders (FGIDs) severity

    Time frame: At 16 weeks of treatment

    Severity index of gastrointestinal symptoms (GI Severity Index, GSI) - Minimum Score: 0 (Indicates absence of gastrointestinal symptoms or optimal bowel regularity) Maximum Score: 17 (Represents the highest severity of symptoms reported in the questionnaire)

Secondary outcomes

  1. Kinetics of Lactobacillus rhamnosus GG (LGG)

    Time frame: At baseline and at 4 weeks, 8 weeks and 12 weeks of treatment

    Using the GI Severity Index (GSI) - Minimum Score: 0 (Indicates absence of gastrointestinal symptoms or optimal bowel regularity) Maximum Score: 17 (Represents the highest severity of symptoms reported in the questionnaire)

  2. Duration of the LGG impact on FGIDs

    Time frame: At baseline and at 4 weeks and 12 weeks from the end of treatment

    Changes in the GSI - Minimum Score: 0 (Indicates absence of gastrointestinal symptoms or optimal bowel regularity) Maximum Score: 17 (Represents the highest severity of symptoms reported in the questionnaire)

  3. Gut Microbiome (GM) composition

    Time frame: At baseline and at 16 weeks of treatment

    Shotgun metagenomics analysis

  4. GM function: fecal short chain fatty acids (SCFAs) levels

    Time frame: At baseline and at 16 weeks of treatment

    Gas chromatograph(GC)-mass spectrometry (MS) analysis

  5. ASD children behavior

    Time frame: At baseline, at 4 weeks, at 8 weeks, at 12 weeks and at 16 weeks of treatment, and at 4 weeks and 12 weeks from the end of treatment

    Aberrant Behavior Checklist (ABC) questionnaire - Minimum Score: 0 (Indicates the complete absence of aberrant or problematic behaviors in the assessed areas, e.g., aggression, social withdrawal, stereotypies, etc.) Maximum Score: 174 (Represents the highest severity and frequency of problematic behaviors reported in the test. All listed aberrant behaviors-such as self-injury, severe hyperactivity, complete social withdrawal, and repetitive speech-are present at maximum intensity.)

  6. Parental quality of life

    Time frame: At baseline, at 4 weeks, at 8 weeks, at 12 weeks and at 16 weeks of treatment, and at 4 weeks and 12 weeks from the end of treatment

    EUROHIS QOL-8 questionnaire - Minimum Score: 8 (Indicates the lowest level of satisfaction and quality of life) Maximum Score: 40 (Indicates the highest level of satisfaction and quality of life)

  7. Body weight

    Time frame: At baseline, at 4 weeks, at 8 weeks, at 12 weeks and at 16 weeks of treatment, and at 4 weeks and 12 weeks from the end of treatment

    Body weight will be evaluated in kilograms

  8. Height

    Time frame: At baseline, at 4 weeks, at 8 weeks, at 12 weeks and at 16 weeks of treatment, and at 4 weeks and 12 weeks from the end of treatment

    Body weight will be evaluated in cm

  9. Infectious diseases

    Time frame: At 4 weeks, at 8 weeks, at 12 weeks and at 16 weeks of treatment, and at 4 weeks and 12 weeks from the end of treatment

    It will be assessed the number of infectious episodes, type of infectious diseases, need for drugs

Sponsors and collaborators

Lead sponsor

Federico II University

Other

Registry information

Acronym: PASD

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Jan 15, 2026
Registry last updated
Jan 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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