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NCT01298622 Clinical Trial

The Imaging Genetic Study of the Core Family of Obsessive-compulsive Disorder (OCD) Patient

OCD Clinical Trial

Official title:
The Study of Structural and Functional Brain Abnormalities and the Association With the Genetic Polymorphism in the Core Family of OCD Patient

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01298622
Other study ID # OCD001
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 2011
Est. completion date December 2022

Study information
Verified date September 2019
Source Kunming Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To investigate the structural/functional abnormalities and the possible genetic endophenotypes of Obsessive-compulsive disorder (OCD) patients and their core families.

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date December 2022
Est. primary completion date December 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 15 Years to 65 Years
Eligibility Inclusion Criteria:

- diagnosed OCD patient

Exclusion Criteria:

- organic disease

- other psychiatric disorder

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
China Psychiatry department of KMC Kunming Yunnan

Sponsors (1)
Lead Sponsor Collaborator
Kunming Medical University

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Y-BOCS Y-BOCS
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