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A medication screening trial evaluation of reserpine, gabapentin and lamotrigine pharmacotherapy of cocaine dependence.

机译:利血平,加巴喷丁和拉莫三嗪药物疗法对可卡因依赖的药物筛选试验评估。

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ABSTRACT Aims To conduct a preliminary evaluation of the safety and efficacy of reserpine, gabapentin or lamotrigine versus an unmatched placebo control as a treatment for cocaine dependence. Design A 10-week out-patient study using the Cocaine Rapid Efficacy and Safety Trial (CREST) study design. Setting The study was conducted at the Cincinnati Medication Development Research Unit (MDRU). Participants Participants met Diagnostic and Statistical Manual version IV (DSM-IV) criteria for cocaine dependence. Sixty participants were enrolled, with 50 participants completing the final study measures. Intervention The targeted daily doses of medication were reserpine 0.5 mg, gabapentin 1800 mg and lamotrigine 150 mg. All participants received 1 hour of manualized individual cognitive behavioral therapy on a weekly basis. Measurements Primary outcome measures of efficacy included urine benzoylecgonine (BE) level, Cocaine Clinical Global Impression scale-observer and self-report of cocaine use. Safety measuresincluded adverse events, electrocardiograms (ECGs), vital signs and laboratory tests. Findings Subjective measures of cocaine dependence indicated significant improvement for all study groups. Urine BE results indicated a significant improvement for the reserpine group (P < 0.05) and non-significant changes for the other study groups. No pattern of physical or laboratory abnormalities attributable to treatment with any of the medications was identified. There were three serious adverse events reported, none of which were related to study procedures. The medications appeared to be tolerated well. Conclusions The present findings suggest that reserpine may be worthy of further study as a cocaine dependence treatment.
机译:摘要目的对利血平,加巴喷丁或拉莫三嗪与无可比拟的安慰剂对照作为可卡因依赖性治疗的安全性和有效性进行初步评估。设计使用可卡因快速疗效和安全性试验(CREST)研究设计进行为期10周的门诊研究。设置该研究在辛辛那提药物开发研究室(MDRU)进行。参与者参与者符合可卡因依赖的诊断和统计手册第四版(DSM-IV)的标准。共有60名参与者参加,其中50名参与者完成了最终的学习措施。干预药物的每日目标剂量是利血平0.5 mg,加巴喷丁1800 mg和拉莫三嗪150 mg。所有参与者每周接受1个小时的手动个性化认知行为治疗。测量疗效的主要结局指标包括尿中苯甲酰芽子碱(BE)水平,可卡因临床总体印象量表观察者和可卡因使用情况的自我报告。安全措施包括不良事件,心电图(ECG),生命体征和实验室检查。结果可卡因依赖性的主观测量表明所有研究组均有显着改善。尿液BE结果表明利血平组有显着改善(P <0.05),其他研究组无显着变化。没有发现可归因于使用任何药物治疗的身体或实验室异常模式。报告了三起严重不良事件,均与研究程序无关。药物似乎耐受良好。结论目前的发现表明利血平作为可卡因依赖治疗可能值得进一步研究。

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