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Clinical Trial Summary

This protocol is a blinded randomized controlled study of the effects of BB-12 with LGG at different doses in 70 healthy children with autism spectrum disorders at lower and higher doses over an 56-day period and a 28- day observation period. The study is being conducted in order to assess safety and tolerability of the probiotic (BB-12 with LGG) at 2 different doses of BB-12 with LGG. Identifying effects on behaviors in healthy children with ASD using SRS-2 and ABC, GI symptoms using GI symptom severity index, and relevant biomarkers of inflammation, microbiota, and metabolites. Primary testing and procedures will be conducted at the University of Texas Health Science Center at Houston and Memorial Hermann. Biomarker identification includes Integrative analysis of plasma metabolome and stool microbiota will be conducted with the collaboration of Dr. Ruth Ann Luna and Dr. Jim Versalovic at Alkek Center for Metagenomics and Microbiome Research, Department of Molecular Virology & Microbiology of Baylor College of Medicine.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03514784
Study type Interventional
Source The University of Texas Health Science Center, Houston
Contact J. Marc Rhoads, MD
Phone 713-500-7642
Email j.marc.rhoads@uth.tmc.edu
Status Recruiting
Phase Phase 1/Phase 2
Start date May 2016
Completion date December 2025

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