Drug Induced Dyskinesia Clinical Trials

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Pathogenesis of Pediatric Obsessive-compulsive Disorder: Based on the Microbiota-gut-brain Axis

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

This study aims to investigate the characteristics of the microbiota-gut-brain axis in pediatric patients with obsessive-compulsive disorder (OCD) through performing an integrated analysis of gut microbiota, serum metabolomics, neuroimaging and electroencephalography (EEG), conducted before and after treatment with selective serotonin reuptake inhibitors (SSRIs). The results will be compared with those of pediatric OCD paitents comorbid with tic disorder (TD) and healthy controls. The findings are expected to further elucidate the potential pathogenesis of OCD, providing a theoretical basis for identifying novel clinical intervention targets and optimizing treatment strategies.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 7
Maximum Age: 17
Healthy Volunteers: t
View:

• (1) 7-17 years old, (2) Y-BOCS score ≥16, (3) with or without a history of TD, (4) Drug-naïve or drug-free for 8 weeks, (5) Wechsler IQ score ≥ 80.

Locations
Other Locations
China
Shanghai Mental Health Center
RECRUITING
Shanghai
Contact Information
Primary
Zhen Wang, PhD, MD
wangzhen@smhc.org.cn
+86 34773516
Backup
Zhen Wang, PhD, MD
wangzhen@smhc.org.cn
+86 64387250
Time Frame
Start Date: 2024-08-24
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 125
Treatments
pediatric OCD patients
Drug-naïve or drug-free pediatric patients with OCD will be enrolled in this group. After data collection, they will receive treatment with SSRIs.
pediatric OCD patients comorbid with TD
Drug-naïve or drug-free pediatric OCD patients comorbid with TD will be enrolled in this group. After data collection, they will receive treatment with SSRIs and antipsychotics.
healthy controls
Healthy children and adolescents will be enrolled in this group for data collection.
Sponsors
Leads: Shanghai Mental Health Center

This content was sourced from clinicaltrials.gov