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DOI 10.1016/j.jsat.2019.08.009

Медицинская библиотека · Journal of substance abuse treatment · 2019

Randomized placebo-controlled trial of galantamine in individuals with cocaine use disorder.

DeVito Elise E, Carroll Kathleen M, Babuscio Theresa, Nich Charla, Sofuoglu Mehmet

СтатьяРандомизированное исследованиеПоддержка NIH: внешняя программаПоддержка правительства СШАПеревод в очереди

Аннотация

No pharmacotherapies are approved for the treatment of cocaine use disorder (CUD). Galantamine, a cholinesterase inhibitor, has shown initial promise for cocaine use reduction in methadone-maintained individuals with CUD and cognitive improvement in abstinent individuals with past CUD. However, galantamine has not previously tested in individuals with current CUD and no comorbid opioid use disorder or methadone maintenance. The goal of this 13-week, double-blind, placebo-controlled, randomized controlled trial was to test the efficacy of galantamine (8 mg or 16 mg/day; extended release (ER)) for reducing cocaine use and improving cognitive function in individuals with cocaine use disorder (CUD). Ninety-three treatment-seeking cocaine users were randomized to placebo (n = 32), 8 mg/day galantamine (n = 31) or 16 mg/day galantamine (n = 30). The medication was well-tolerated with minimal reports of side-effects. However, there were no significant treatment group differences in cocaine use outcomes (as measured by self-report or urines). The 16 mg galantamine group had a greater improvement in working memory capacity (Backwards Digit Span), but there were no other significant treatment group differences on key cognitive outcomes. These findings did not provide support for the efficacy of galantamine as a treatment for cocaine use in this sample of individuals with CUD.

Для цитирования: DeVito Elise E, Carroll Kathleen M, Babuscio Theresa, Nich Charla, Sofuoglu Mehmet. Randomized placebo-controlled trial of galantamine in individuals with cocaine use disorder.. Journal of substance abuse treatment. 2019. DOI: 10.1016/j.jsat.2019.08.009.

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