Treating Schizophrenia by Correcting Abnormal Brain Development

Beth Israel Lahey Health

Status and phase: Active, not recruiting; Phase 3

Conditions: Schizophrenia

Treatments: Drug: Tiagabine; Drug: Placebo

Study type: Interventional

Funder types: Other

Identifiers

NCT00179465

2004P000078

Details and patient eligibility

About

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.

Full description

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.

Enrollment: 36 estimated patients

Sex: All

Ages: 18 to 25 years old

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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36 participants in 2 patient groups, including a placebo group

Antipsychotic plus study drug

Active Comparator group

Description:

Half of the subjects will receive the study medications in addition to their ongoing antipsychotic regimen.

Treatment:

Drug: Tiagabine

Antipsychotics plus placebo

Placebo Comparator group

Description:

Half of the subjects will receive placebo in addition to their antipsychotic regimen.

Treatment:

Drug: Placebo