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.
PROTOCOL OUTLINE: All patients are screened with a complete physical and neurologic exam,
and a semi-structured interview. Patients then receive a comprehensive assessment of
systemic disease. Patients and first-degree family members also participate in a genetic
study.
Any patient who experiences an unusual exacerbation of symptoms or significant side effects
is removed from the study.
;
Primary Purpose: Screening
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
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||
| Completed |
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N/A | |
| Completed |
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|
Phase 1 | |
| Completed |
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|
N/A | |
| Terminated |
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|
Phase 1 | |
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N/A | |
| Completed |
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|
Phase 3 | |
| Completed |
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|
Phase 3 | |
| Completed |
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|
N/A | |
| Completed |
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Role of the Sensory Experience in Generating Motor Tics in Tourette Syndrome
|
||
| Completed |
NCT03325010 -
Safety, Tolerability, and Efficacy of NBI-98854 for the Treatment of Pediatric Subjects With Tourette Syndrome
|
Phase 2 | |
| Not yet recruiting |
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Sertraline vs. Placebo in the Treatment of Anxiety in Children and AdoLescents With NeurodevelopMental Disorders
|
Phase 2 | |
| Completed |
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Neurofeedback for Tourette Syndrome
|
N/A | |
| Completed |
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|
Phase 1 | |
| Completed |
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|
Phase 2 | |
| Completed |
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|
Phase 3 | |
| Terminated |
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|
Phase 2 |