Tourette Syndrome Clinical Trial
OBJECTIVES: I. Investigate the pathobiology of Tourette syndrome and related disorders by
measuring various compounds of interest in cerebrospinal fluid, plasma, and urine of
patients with Tourette syndrome, obsessive compulsive disorder, and/or chronic tics.
II. Determine the pattern of familial aggregation of Tourette syndrome and obsessive
compulsive disorder by systematic assessment of all first-degree family members of patients
selected for cerebrospinal fluid studies.
III. Establish the neurochemical and neuropeptide profile associated with the range of
expression of the putative Tourette gene expression in adult and adolescent patients.
Status | Completed |
Enrollment | 200 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 12 Years to 45 Years |
Eligibility |
PROTOCOL ENTRY CRITERIA: --Disease Characteristics-- Diagnostic and Statistical Manual of Mental Disorders IV lifetime diagnosis of 1 or more of the following: - Tourette syndrome (TS) - Obsessive compulsive disorder - Chronic tics Severely affected adolescents with a score of 3 or greater on the TS-Clinical Global Impression Scale eligible --Prior/Concurrent Therapy-- At least 1 month since any medication --Patient Characteristics-- Other: - In good physical health - No alcohol or substance abuse - No Intelligence Quotient below 80 - Negative pregnancy test required of fertile women |
Primary Purpose: Screening
Country | Name | City | State |
---|---|---|---|
United States | Yale University School of Medicine | New Haven | Connecticut |
Lead Sponsor | Collaborator |
---|---|
National Center for Research Resources (NCRR) | Yale University |
United States,
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* Note: There are 22 references in all — Click here to view all references
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