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Combination of Modafinil and d-amphetamine for the Treatment of Cocaine Dependence: A Preliminary Investigation
Background: Two stimulant medications, modafinil and d-amphetamine, when tested individually, have shown safety and efficacy for treatment of cocaine addiction. We hypothesized that the combination of modafinil and d-amphetamine, at low doses, would show equivalent or greater benefit in reducing coc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Research Foundation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430875/ https://www.ncbi.nlm.nih.gov/pubmed/22969732 http://dx.doi.org/10.3389/fpsyt.2012.00077 |
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author | Schmitz, Joy M. Rathnayaka, Nuvan Green, Charles E. Moeller, F. Gerard Dougherty, Anne E. Grabowski, John |
author_facet | Schmitz, Joy M. Rathnayaka, Nuvan Green, Charles E. Moeller, F. Gerard Dougherty, Anne E. Grabowski, John |
author_sort | Schmitz, Joy M. |
collection | PubMed |
description | Background: Two stimulant medications, modafinil and d-amphetamine, when tested individually, have shown safety and efficacy for treatment of cocaine addiction. We hypothesized that the combination of modafinil and d-amphetamine, at low doses, would show equivalent or greater benefit in reducing cocaine use compared to higher doses of each individual medication or placebo. Methods: Sixteen week, randomized, parallel-group design with four treatment arms comparing placebo to modafinil 400 mg; d-amphetamine 60 mg; modafinil 200 mg plus d-amphetamine 30 mg. Primary outcome variables, retention and cocaine use, were analyzed on the sample of 73 participants who received the first dose of the study medication. Results: Retention rates did not differ between groups and were generally low, with 40% remaining in treatment at week 12 and 20% at week 16. Participants receiving the combination of modafinil and d-amphetamine showed a trend of increased cocaine use over time with a corresponding low Bayesian probability of benefit (33%). Relatively better cocaine outcomes were observed in the placebo and d-amphetamine only groups. The study medications were generally well-tolerated with few adverse effects, yet rates of adherence were suboptimal (≤80%). Conclusion: Data from this preliminary investigation fail to provide evidential support for conducting a larger study of this dual-agonist medication combination for treatment of cocaine dependence. |
format | Online Article Text |
id | pubmed-3430875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-34308752012-09-11 Combination of Modafinil and d-amphetamine for the Treatment of Cocaine Dependence: A Preliminary Investigation Schmitz, Joy M. Rathnayaka, Nuvan Green, Charles E. Moeller, F. Gerard Dougherty, Anne E. Grabowski, John Front Psychiatry Psychiatry Background: Two stimulant medications, modafinil and d-amphetamine, when tested individually, have shown safety and efficacy for treatment of cocaine addiction. We hypothesized that the combination of modafinil and d-amphetamine, at low doses, would show equivalent or greater benefit in reducing cocaine use compared to higher doses of each individual medication or placebo. Methods: Sixteen week, randomized, parallel-group design with four treatment arms comparing placebo to modafinil 400 mg; d-amphetamine 60 mg; modafinil 200 mg plus d-amphetamine 30 mg. Primary outcome variables, retention and cocaine use, were analyzed on the sample of 73 participants who received the first dose of the study medication. Results: Retention rates did not differ between groups and were generally low, with 40% remaining in treatment at week 12 and 20% at week 16. Participants receiving the combination of modafinil and d-amphetamine showed a trend of increased cocaine use over time with a corresponding low Bayesian probability of benefit (33%). Relatively better cocaine outcomes were observed in the placebo and d-amphetamine only groups. The study medications were generally well-tolerated with few adverse effects, yet rates of adherence were suboptimal (≤80%). Conclusion: Data from this preliminary investigation fail to provide evidential support for conducting a larger study of this dual-agonist medication combination for treatment of cocaine dependence. Frontiers Research Foundation 2012-08-30 /pmc/articles/PMC3430875/ /pubmed/22969732 http://dx.doi.org/10.3389/fpsyt.2012.00077 Text en Copyright © 2012 Schmitz, Rathnayaka, Green, Moeller, Dougherty and Grabowski. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Psychiatry Schmitz, Joy M. Rathnayaka, Nuvan Green, Charles E. Moeller, F. Gerard Dougherty, Anne E. Grabowski, John Combination of Modafinil and d-amphetamine for the Treatment of Cocaine Dependence: A Preliminary Investigation |
title | Combination of Modafinil and d-amphetamine for the Treatment of Cocaine Dependence: A Preliminary Investigation |
title_full | Combination of Modafinil and d-amphetamine for the Treatment of Cocaine Dependence: A Preliminary Investigation |
title_fullStr | Combination of Modafinil and d-amphetamine for the Treatment of Cocaine Dependence: A Preliminary Investigation |
title_full_unstemmed | Combination of Modafinil and d-amphetamine for the Treatment of Cocaine Dependence: A Preliminary Investigation |
title_short | Combination of Modafinil and d-amphetamine for the Treatment of Cocaine Dependence: A Preliminary Investigation |
title_sort | combination of modafinil and d-amphetamine for the treatment of cocaine dependence: a preliminary investigation |
topic | Psychiatry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430875/ https://www.ncbi.nlm.nih.gov/pubmed/22969732 http://dx.doi.org/10.3389/fpsyt.2012.00077 |
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