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| Name | Class |
|---|---|
| Provincial Health Services Authority British Columbia | OTHER |
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This is a 15 week trial to determine (1) the safety and tolerability of varenicline when used for smoking cessation/reduction in individuals with schizophrenia; (2) if treatment with varenicline affects the symptoms of schizophrenia.
Researchers are looking to recruit a total of 50 subjects at Riverview and Forensic Psychiatric Hospitals who would like to reduce or quit smoking cigarettes. This open label pilot study will gather information regarding the safety and tolerability of varenicline in subjects who have been diagnosed with schizophrenia or schizoaffective disorder. Consenting subjects will be prescribed varenicline as follows: varenicline 0.5 mg/d for days 1 to 3, 0.5 mg twice daily for days 4 to 7, then 1 mg twice daily through week 12. The research team will meet with the subject once a week for twelve weeks and the subject will be interviewed and asked to complete questionnaires about his/her psychiatric symptoms, tobacco use and nicotine dependence. The measures used include the FTND, PANSS, CGI-I, CGI-S, ESRS, UKU, BARS, WSWS, QSU-brief, mCEQ, and the OAS-M. The CGI-SS will also be completed throughout the study as well as once weekly for three weeks following the completion of the study (Post-Study follow-up visits 1-3).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Experimental | Smoking cessation drug - varenicline |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Varenicline | Drug | Varenicline 0.5 mg/d for days 1 to 3, 0.5 mg twice daily for days 4 to 7, then 1 mg twice daily through week 12. Administration of twice daily dosing should be at least 8 hours apart. |
| Measure | Description | Time Frame |
|---|---|---|
| Changes in the symptoms of the primary illness. These outcomes will be measured at study visits 1, 2, 4, 8, and 12. | 12 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Safety and tolerability, nicotine dependence, and smoking cessation/reduction. These outcomes will be measured at study visits 1-12. | 12 weeks |
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Inclusion Criteria:
Exclusion Criteria:
Clinically significant allergic reactions to the study medication
Clinically significant abnormalities in the screening laboratory values
Subjects at significant risk of self-harm
Previous treatment with varenicline
Women who are pregnant, breast-feeding, or of child-bearing potential not using adequate contraception
Men not using adequate contraception
Use of medications that might interfere with the study medication evaluation
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| Name | Affiliation | Role |
|---|---|---|
| Ric M. Procyshyn, Ph.D | University of British Columbia | Principal Investigator |
| Alasdair Barr, Ph.D | University of British Columbia | Study Director |
| Joyce Coutts, MD | Forensic Psychiatric Institute | Study Director |
| Sean Flynn, MD | University of British Columbia | Study Director |
| Chris Schenk, MD | Riverview Hospital | Study Director |
| William Honer, MD | University of British Columbia | Study Director |
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| ID | Term |
|---|---|
| D012559 | Schizophrenia |
| D011618 | Psychotic Disorders |
| D016540 | Smoking Cessation |
| D014029 | Tobacco Use Disorder |
| ID | Term |
|---|---|
| D019967 | Schizophrenia Spectrum and Other Psychotic Disorders |
| D001523 | Mental Disorders |
| D015438 | Health Behavior |
| D001519 | Behavior |
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| ID | Term |
|---|---|
| D000068580 | Varenicline |
| ID | Term |
|---|---|
| D001552 | Benzazepines |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |
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|
| D019966 | Substance-Related Disorders |
| D064419 | Chemically-Induced Disorders |
| D011810 | Quinoxalines |