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The purpose of this study is to determine whether topiramate is effective as an aid to smoking cessation for recovering alcohol dependent men.
This study is a 12-week, double-blind, placebo-controlled trial to test the efficacy of topiramate versus placebo as an aid to smoking cessation for recovering alcohol dependent men. Another aim of the study is to explore whether or not topiramate reduces relapse to alcohol use in patients with comorbid alcohol and nicotine dependence. All participants will receive a standardized psychosocial intervention in combination with the medication (or placebo). Following completion of the treatment phase of the study, participants will enter a 24-week follow-up period during which the longer-term outcome of the intervention will be assessed.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Topiramate | Other | The subjects for the proposed study will be 180 currently smoking, treatment-seeking male veterans with alcohol and nicotine dependence. Ninety subjects will be randomized to the topiramate arm and 90 subjects will be randomized to the placebo group. |
|
| Placebo | Placebo Comparator | 90 participants, will receive matching placebo |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Topiramate | Drug | Topiramate will be titrated over 5 weeks to a maximum dosage of 200 mg according to the following schedule: 25mg daily for days 1-7, 50mg daily for days 8-14, 75mg daily for days 15-21, 100mg daily for days 22-28, 150mg daily for days 29-35, 200mg daily for days 36-42. Maximum dosage will be maintained for 6 weeks, followed by a one-week taper-off period (100mg daily for 4 days and 50mg daily for 3 days). |
| Measure | Description | Time Frame |
|---|---|---|
| 4-week Continuous Abstinence From Smoking | This measure indicates the proportion of participants who did or did not smoke any cigarettes during the final 4 weeks of treatment, which represented weeks 8-12 of study participation. | Weeks 8-12 of treatment. |
| Measure | Description | Time Frame |
|---|---|---|
| Percent Relapsing to Any Drinking or Illicit Drug Use | Alcohol or illicit drug use during treatment or follow up. | 12-week treatment phase, 36-week combined treatment and follow-up |
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Inclusion Criteria:
Subjects will be included if they:
Exclusion Criteria:
Subjects will be excluded if they:
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| Name | Affiliation | Role |
|---|---|---|
| Robert M. Anthenelli, MD | VA San Diego Healthcare System, San Diego, CA | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| VA San Diego Healthcare System, San Diego, CA | San Diego | California | 92161 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 28029173 | Derived | Anthenelli RM, Heffner JL, Wong E, Tibbs J, Russell K, Isgro M, Dinh E, Wehrle C, Worley MJ, Doran N. A Randomized Trial Evaluating Whether Topiramate Aids Smoking Cessation and Prevents Alcohol Relapse in Recovering Alcohol-Dependent Men. Alcohol Clin Exp Res. 2017 Jan;41(1):197-206. doi: 10.1111/acer.13279. Epub 2016 Dec 28. |
| Label | URL |
|---|---|
| Click here for more information about this study: Topiramate to Aid Smoking Cessation in Recovering Alcohol Dependent Men | View source |
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| ID | Title | Description |
|---|---|---|
| FG000 | Topiramate | The subjects for the proposed study will be 180 currently smoking, treatment-seeking male veterans with alcohol and nicotine dependence. Ninety subjects will be randomized to the topiramate arm and 90 subjects will be randomized to the placebo group. Topiramate: Topiramate will be titrated over 5 weeks to a maximum dosage of 200 mg according to the following schedule: 25mg daily for days 1-7, 50mg daily for days 8-14, 75mg daily for days 15-21, 100mg daily for days 22-28, 150mg daily for days 29-35, 200mg daily for days 36-42. Maximum dosage will be maintained for 6 weeks, followed by a one-week taper-off period (100mg daily for 4 days and 50mg daily for 3 days). |
| FG001 | Placebo | 90 participants, will receive matching placebo Placebo: Placebo/study medication will be administered in opaque capsules in an identical fashion to maintain the double-blind study design. |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Topiramate | Received active topiramate |
| BG001 | Placebo | Received placebo |
| BG002 |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | 4-week Continuous Abstinence From Smoking | This measure indicates the proportion of participants who did or did not smoke any cigarettes during the final 4 weeks of treatment, which represented weeks 8-12 of study participation. | Posted | Number | percentage of participants abstinent | Weeks 8-12 of treatment. |
|
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Topiramate |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| alcohol relapse with suicidal ideation | Psychiatric disorders | Non-systematic Assessment | 1 participant in the topiramate group experienced an alcohol relapse that included suicidal ideation. |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Upper respiratory infection | Respiratory, thoracic and mediastinal disorders | Non-systematic Assessment |
Dually-dependent male smokers with high rates of SUDs and psychiatric disorders, thus not generalizable to other populations; topiramate dose lower than the dose found to reduce smoking in active alcoholics; attrition may have impacted results.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Neal Doran, PhD | VA San Diego | 8585528585 | 2421 | neal.doran@va.gov |
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| ID | Term |
|---|---|
| D014029 | Tobacco Use Disorder |
| D000437 | Alcoholism |
| ID | Term |
|---|---|
| D019966 | Substance-Related Disorders |
| D064419 | Chemically-Induced Disorders |
| D001523 | Mental Disorders |
| D019973 | Alcohol-Related Disorders |
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| ID | Term |
|---|---|
| D000077236 | Topiramate |
| ID | Term |
|---|---|
| D005632 | Fructose |
| D006601 | Hexoses |
| D009005 | Monosaccharides |
| D000073893 | Sugars |
| D002241 |
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|
|
| Placebo | Drug | Placebo/study medication will be administered in opaque capsules in an identical fashion to maintain the double-blind study design. |
|
| Total |
Total of all reporting groups |
| years |
|
| Gender | Count of Participants | Participants |
|
| Race/Ethnicity, Customized | Number | participants |
|
| Region of Enrollment | Number | participants |
|
| Fagerstrom | Scores on the Fagerstrom Test for Nicotine Dependence range from 0 to 10, with higher scores indicating greater nicotine dependence. | Mean | Standard Deviation | units on a scale |
|
| Units | Counts |
|---|---|
| Participants |
|
|
| Secondary | Percent Relapsing to Any Drinking or Illicit Drug Use | Alcohol or illicit drug use during treatment or follow up. | Posted | Number | percentage of participants | 12-week treatment phase, 36-week combined treatment and follow-up |
|
|
|
|
| 1 |
| 63 |
| 46 |
| 63 |
| EG001 | Placebo | 3 | 66 | 49 | 66 |
|
| alcohol relapse | Psychiatric disorders | Non-systematic Assessment | 2 participants in the placebo group experienced relapses to alcohol |
|
| atrial fibrillation | Cardiac disorders |
|
| Headache | General disorders | Non-systematic Assessment |
|
| Paresthesia | Nervous system disorders | Systematic Assessment |
|
| Loss of appetite | General disorders | Non-systematic Assessment |
|
| Reduced concentration | Psychiatric disorders | Non-systematic Assessment |
|
| Dysgeusia | General disorders | Non-systematic Assessment |
|
| Dizziness | General disorders | Non-systematic Assessment |
|
| Back pain | Musculoskeletal and connective tissue disorders | Non-systematic Assessment |
|
| Somnolence | General disorders | Non-systematic Assessment |
|
| Depression | Psychiatric disorders | Systematic Assessment |
|
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| Carbohydrates |
| D007661 | Ketoses |
| Hazard Ratio (HR) |
| 1.30 |
| 2-Sided |
| 95 |
| 0.66 |
| 2.55 |
| No |
| Superiority or Other |