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NCT Number: NCT06352203

Effect of Probiotics on the Intestinal Microbiota of Pediatric Patients

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.

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Key information

Age range

3 year–7 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hospital Universitario Infantil Niño Jesús

Madrid, Spain

Location status: Recruiting

Location contact

Silvia Gutierrez, MD

CONTACT

[email protected]

+34918035179

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Children aged 3 to 7 years old.
  • Diagnosed with autism spectrum disorder, according to the clinical criteria of the "Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5)" and who meet criteria for ASD according to the ADOS-2 classification.
  • Presenting one or more gastrointestinal symptoms (constipation, diarrhoea, abnormal stools, painful defecation, abdominal pain, reflux, bloating, flatulence).
  • Written informed consent signed by the parent or legal guardian with express or tacit consent of the other parent.

Exclusion criteria

  • With intake of antibiotics in the last month.
  • With intake of probiotics in the last two weeks.
  • Diagnosed with short bowel syndrome or has undergone relevant surgery on the gastrointestinal tract.
  • Exhibiting a defect in the intestinal epithelial barrier (e.g. inflammatory bowel disease (IBD)).
  • Diagnosed with endocrinological diseases such as diabetes mellitus, hypo- and hyperthyroidism, Cushing's disease, Addison's disease, etc.
  • Having heart failure and a cardiac medical history (e.g. artificial heart valve, medical history of infective endocarditis, rheumatic fever, or cardiac malformation).
  • Congenital or acquired immunodeficiency.
  • Immunocompromised (e.g., cancer and/or transplant patients taking certain immunosuppressive drugs, patients with inherited diseases that affect or may affect the immune system).
  • Uncertainty on the part of the investigator about the willingness or ability of the minor's parents or legal guardian to comply with the requirements of the protocol.
  • With oral hyper sensitivity impairments that prevent the uptake of the study product.

Treatment and study plan

Probiotic

Dietary Supplement

1 dose of the probiotic every 24 hours, for 6-months.

Placebo

Dietary Supplement

1 dose of the placebo every 24 hours, for 6-months.

Primary outcomes

  1. Number of children with intestinal dysbiosis after 6 months of treatment.

    Time frame: After 6 months of intervention.

Study contacts

Contact information is provided by the study sponsor or research team.

Susana Manzano Jiménez, PhD

CONTACT

[email protected]

+34 918035179

Sponsors and collaborators

Lead sponsor

ProbiSearch SL

Industry

Registry information

Official study title

Randomized, Double-blind, Placebo-controlled Study to Evaluate the Modulating Effect of Probiotics on the Intestinal Microbiota of Pediatric Patients With Neurodevelopmental Disorders.

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Apr 8, 2024
Registry last updated
Feb 25, 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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