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随机、双盲、安慰剂对照试验莫达非尼治疗甲基苯丙胺依赖。

Randomized, double-blind, placebo-controlled trial of modafinil for the treatment of methamphetamine dependence.

机构信息

Department of Family Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA.

出版信息

Drug Alcohol Depend. 2010 Jun 1;109(1-3):20-9. doi: 10.1016/j.drugalcdep.2009.11.023. Epub 2010 Jan 25.

Abstract

OBJECTIVE

To compare modafinil to placebo for reducing methamphetamine (MA) use, improving retention, and reducing depressive symptoms and MA cravings. Rates of adverse events and cigarette smoking with modafinil versus placebo were also compared.

METHODS

Following a 2-week, non-medication lead-in period, 71 treatment-seeking MA-dependent participants were randomly assigned to modafinil (400mg once daily; N=34) or placebo (once daily; N=37) for 12 weeks under double-blind conditions. Participants attended clinic thrice-weekly to provide urine samples analyzed for MA-metabolite, to complete research assessments, and to receive contingency management and weekly cognitive behavioral therapy (CBT) sessions.

RESULTS

There were no statistically significant effects for modafinil on MA use, retention, depressive symptoms, or MA cravings in pre-planned analyses. Outcomes for retention and MA use favored modafinil in a post hoc analysis among participants with low CBT attendance and among participants with baseline high-frequency of MA use (MA use on >18 of past 30 days), but did not reach statistical significance in these small subgroups. Modafinil was safe and well tolerated and did not increase cigarette smoking.

CONCLUSIONS

Modafinil was no more effective than placebo at 400mg daily in a general sample of MA users. A post hoc analysis showing a trend favoring modafinil among subgroups with baseline high-frequency MA use and low CBT attendance suggests that further evaluation of modafinil in MA users is warranted.

摘要

目的

比较莫达非尼与安慰剂在减少甲基苯丙胺(MA)使用、提高保留率、减少抑郁症状和 MA 渴望方面的效果。还比较了莫达非尼与安慰剂的不良反应发生率和吸烟率。

方法

在为期 2 周的非药物导入期后,71 名寻求治疗的 MA 依赖参与者被随机分配接受莫达非尼(400mg 每日一次;N=34)或安慰剂(每日一次;N=37)治疗,为期 12 周,采用双盲条件。参与者每三周到诊所提供尿液样本进行 MA 代谢物分析,完成研究评估,并接受应急管理和每周认知行为疗法(CBT)。

结果

在预先计划的分析中,莫达非尼对 MA 使用、保留率、抑郁症状或 MA 渴望均无统计学显著影响。在低 CBT 出勤率的参与者和基线 MA 使用频率高(过去 30 天中有 >18 天使用 MA)的参与者的事后分析中,莫达非尼对保留率和 MA 使用的结果更为有利,但在这些小亚组中未达到统计学意义。莫达非尼安全且耐受性良好,不会增加吸烟。

结论

在一般 MA 用户样本中,莫达非尼 400mg 每日一次的效果并不优于安慰剂。事后分析显示,在基线 MA 使用频率高和 CBT 出勤率低的亚组中,莫达非尼有趋势有利,这表明进一步评估莫达非尼在 MA 用户中的应用是有必要的。

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