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Effects of Lactobacillus Plantarum PS128 in Patients With Tourette's Syndrome

Tourette's Syndrome Clinical Trial

Official title:
Effects of Lactobacillus Plantarum PS128 in Patients With Tourette's Syndrome

Clinical Trial Summary

To evaluate whether supplementing with PS128 can improve the symptoms and quality of life related to Tourette's disease in children.

Clinical Trial Description

This is a randomized double-blind healthy control study and the implementation period is after Institutional Review Board (IRB) approval to December 31, 2022. Experimental group: 80 subjects who meet the criteria for the admission of Tourette's disease will be enrolled. They will consume the PS128 or placebo capsules every day, 2 capsules at a time, for 12 weeks. Healthy control group: 40 subjects of the same age as the experimental group will be included, without any intervention measures, only collect stool sample once. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04805385
Study type Interventional
Source China Medical University Hospital
Contact I-Ching Chou, MD
Phone +886 4 22052121
Email iching@mail.cmu.edu.tw
Status Recruiting
Phase N/A
Start date November 29, 2021
Completion date December 31, 2022
View Details
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