Expired Study
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Boston, Massachusetts 02115


Purpose:

The purpose of this study is to determine whether treatment with tiagabine (Gabitril) during the early course of schizophrenia can fundamentally correct the brain deficits associated with the disease. This study is funded by the National Institutes of Health.


Study summary:

It is hypothesized that enhancement of GABA neurotransmission during the early course of the illness by tiagabine (Gabitril), a GABA transporter GAT-1-specific inhibitor and a FDA-approved anticonvulsant, will improve both clinical symptoms and working memory in schizophrenia. This improvement is postulated to be the result of tiagabine-mediated modification of the developmental synaptic pruning of prefrontal cortical circuitry. The occurrence of circuitry modification after tiagabine treatment will be assessed by the following independent methodologic approaches: MRI morphometric analysis of prefrontal gray matter volume and fMRI measurements of brain activity patterns during performance of tasks that probe working memory.


Criteria:

Inclusion Criteria: - Meets criteria for the diagnosis of schizophrenia, with onset of psychotic symptoms within the past 3 years. - Currently on second-generation antipsychotics for at least 3 months. - Age 18-25, otherwise healthy. Exclusion Criteria: - Diagnosis of schizoaffective disorder. - Has failed two or more clinically adequate antipsychotic trials. - History of seizures or any neurologic disorders. - Pregnant or nursing women. - Known HIV infection. - Actively suicidal. - History of any substance dependence. - Currently meets criteria for substance abuse/dependence. - Other MRI exclusion criteria per Radiology Department protocols.


NCT ID:

NCT00179465


Primary Contact:

Principal Investigator
T.-U. Wilson Woo, M.D., Ph.D.
Beth Israel Deaconess Medical Center, Harvard Medical School


Backup Contact:

N/A


Location Contact:

Boston, Massachusetts 02115
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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