Clinical Trials Directory

Trials / Completed

CompletedNCT04805385

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
121 (actual)
Sponsor
China Medical University Hospital · Academic / Other
Sex
All
Age
4 Years – 18 Years
Healthy volunteers
Accepted

Summary

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

Detailed description

This is a randomized double-blind healthy control study and the implementation period is after Institutional Review Board (IRB) approval to December 31, 2023. 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.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTPS128Each PS128 capsule contained \>1 × 10\^10 colony forming units (CFU) with microcrystalline cellulose and weights 425 ± 25 mg The placebo capsules only contained 425 ± 25 mg microcrystalline cellulose

Timeline

Start date
2021-11-29
Primary completion
2023-12-31
Completion
2023-12-31
First posted
2021-03-18
Last updated
2026-01-29

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT04805385. Inclusion in this directory is not an endorsement.

Effects of Lactobacillus Plantarum PS128 in Patients With Tourette's Syndrome (NCT04805385) · Clinical Trials Directory