The Imaging Genetic Study of the Core Family of Obsessive-compulsive Disorder (OCD) Patient
- Conditions
- OCD
- Registration Number
- NCT01298622
- Lead Sponsor
- Kunming Medical University
- Brief Summary
To investigate the structural/functional abnormalities and the possible genetic endophenotypes of Obsessive-compulsive disorder (OCD) patients and their core families.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
- diagnosed OCD patient
Exclusion Criteria
- organic disease
- other psychiatric disorder
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Y-BOCS Y-BOCS
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What genetic polymorphisms are associated with structural brain abnormalities in OCD families?
How do functional MRI findings in NCT01298622 correlate with known OCD biomarkers like 5-HT2A receptor activity?
What molecular pathways link OCD endophenotypes to striatal volume changes observed in this study?
Are there comparative effectiveness studies of deep brain stimulation vs standard SSRIs in treatment-resistant OCD families?
What adverse event profiles are reported in genetic-based OCD studies using neuroimaging biomarkers?
Trial Locations
- Locations (1)
Psychiatry department of KMC
🇨🇳Kunming, Yunnan, China
Psychiatry department of KMC🇨🇳Kunming, Yunnan, ChinaXiufeng Xu, MD.Contactxfxu2004@sina.com.cnYuqi Cheng, PhDPrincipal Investigator