Actively Recruiting
Washed Microbiota Transplantation for Tourette's Syndrome
Led by The Second Hospital of Nanjing Medical University · Updated on 2024-08-19
30
Participants Needed
2
Research Sites
184 weeks
Total Duration
On this page
Sponsors
T
The Second Hospital of Nanjing Medical University
Lead Sponsor
N
Nanjing Medical University
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study aimed to evaluate the efficacy of washed microbiota transplantation in the treatment of Tourette's syndrome (TS).
CONDITIONS
Official Title
Washed Microbiota Transplantation for Tourette's Syndrome
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 6 to 17 years (inclusive)
- Diagnosed with Tourette's Syndrome based on DSM-5 criteria
- Yale Global Tic Severity Scale-Total Tic Score (YGTSS-TTS) of at least 20 at screening and baseline
- Undergoing washed microbiota transplantation (WMT) treatment
You will not qualify if you...
- Having brain diseases such as tumors, injuries, or cerebrovascular disease
- Having severe diseases including cancers, organ failure, or heart diseases
- Exhibiting stereotypy linked to autism spectrum disorder
- Diagnosed with psychiatric disorders like bipolar disorder, schizophrenia, or major depression
- Having clinically significant obsessive-compulsive disorder as the main cause of impairment
- Using medications that affect gut microbiota such as antibiotics or probiotics within three months before WMT
- Having neurological disorders other than Tourette's Syndrome that could affect tic evaluation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Department of Microbiota Medicine & Medical Centre for Digestive Diseases, The Second Affiliated Hospital of Nanjing Medical University
Nanjing, Jiangsu, China, 210011
Actively Recruiting
2
SIR RUN RUN hospital of Nanjing Medical University
Nanjing, Jiangsu, China, 210011
Actively Recruiting
Research Team
F
Faming Zhang, MD; PHD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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