Schizophrenia Clinical Trial
— VAR-PASOfficial title:
Effects of Varenicline on Cortical Neuroplasticity and Working Memory in Patients With Schizophrenia and Healthy Controls
Verified date | August 2015 |
Source | Centre for Addiction and Mental Health |
Contact | n/a |
Is FDA regulated | No |
Health authority | Canada: Health Canada |
Study type | Interventional |
This laboratory pilot study will explore the effects of varenicline tartrate on long-term potentiation (LTP)-like mechanisms of (1) the motor cortex and (2) the dorsolateral prefrontal cortex (DLPFC) and working memory in non-smoking patients with schizophrenia and healthy controls using a Paired Associative Stimulation (PAS) method. The present study will use this novel PAS method to evaluate the effects of five doses of varenicline (Champix) 0.5 mg BID treatment on neuroplasticity changes and working memory in 28 non-smokers with schizophrenia and 28 non-smoking controls in a placebo-controlled, double-blinded, cross-over design. The hypothesis is that varenicline will increase LTP-like facilitation of the DLPFC as compared with placebo in patients with schizophrenia, with less or a null effect in healthy controls. Likewise, it is hypothesized that varenicline will specifically improve working memory in patients with schizophrenia as compared with placebo and healthy controls. We Hypothesize that: 1.Patients with Schizophrenia(SCZ) will have reduced cortical LTP and impaired working memory compared to healthy controls 2. Sub-chronic varenicline challenge will attenuate the cortical LTP and working memory deficit in patients with SCZ. 3.Reversal of the cortical LTP deficit by varenicline in patients with SCZ will be associated with improvement in working memory.
Status | Completed |
Enrollment | 24 |
Est. completion date | August 2015 |
Est. primary completion date | August 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 55 Years |
Eligibility |
Inclusion Criteria (Healthy subjects and Scz): - Non-smoker or past smoker, abstinent for at least the last 1 year - Females with potential childbearing must have a negative serum pregnancy test at inclusion. - Ability and willingness to speak English - Willingness to provide informed consent - Adequate hearing and visual capacity, or corrected by visual/ hearing aid, right handedness. INCLUSION Criteria (Scz Only): - Diagnosis of schizophrenia - Stable psychotropic drug treatment for at least the past 4 weeks - Clinically stable for the past 3 months. Exclusion Criteria (healthy subjects and SCZ): - Current smoker or abstinent smoker for less than 1 year - Current history of drug abuse disorder or current elicit drug use - Current or past history of neurological disorder - Current or past history of seizures - Any metal implants - Mini Mental Status Examination score of less than 20 - Diagnosis of bipolar disorder or current Major depression episode - Electroconvulsive Therapy (ECT) within 6 months - Varenicline hypersensitivity. |
Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator)
Country | Name | City | State |
---|---|---|---|
Canada | Centre for Addiction and Mental Health | Toronto | Ontario |
Lead Sponsor | Collaborator |
---|---|
Centre for Addiction and Mental Health | Pfizer |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change of Paired Associative Stimulation (PAS) induced plasticity from baseline | Day 3 of weeks 1 and 2 | No | |
Secondary | Change of Working memory performance from baseline | Day 3 of weeks 1 and 2 | No |
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