Shoptaw Steven, Watson Donnie W, Reiber Chris, Rawson Richard A, Montgomery Margaret A, Majewska Maria D, Ling Walter
UCLA Integrated Substance Abuse Programs, Los Angeles, CA 90025, USA.
Addiction. 2005 Mar;100 Suppl 1:78-90. doi: 10.1111/j.1360-0443.2005.00991.x.
This study tested three dopaminergic medications against a common unmatched placebo condition: hydergine 1 mg three times daily (n = 15); levodopa/carbidopa 25/100 mg three times daily (n = 15); cabergoline 0.5 mg per week (n = 15); and placebo three times daily (n = 15) as potential pharmacotherapies for cocaine dependence.
The four-parallel group, Cocaine Rapid Efficacy Screening Trial (CREST) design featured a 2-week baseline period followed by randomization to an 8-week medication condition that included 1 hour per week of cognitive behavioral drug counseling. A safety evaluation was conducted 4 weeks after termination.
Outcomes included cocaine metabolites measured in urine, retention and self-reports for drug use, cocaine craving, clinical improvement, mood and HIV risk behaviors.
Participants assigned to receive cabergoline provided more urine samples negative for cocaine metabolites (42.4%) than those assigned to receive placebo (25.0%), a statistically significant difference after controlling for baseline differences in self-reported cocaine use (F = 2.95, df = 3; P = 0.05). Cabergoline-treated participants demonstrated a significant improvement over placebo from baseline to week 8 when measured using the Addiction Severity Index (ASI) employment subscale (overall change = - 0.09, SD = 0.10, t = 2.36, P < 0.05). Safety and adverse event measures showed similar rates and types of complaints by treatment condition.
These results, combined with the apparent safety of cabergoline when used with this population, provide empirical support for conducting a larger study of the medication.
本研究针对一种常见的非匹配安慰剂对照情况,测试了三种多巴胺能药物:喜得镇1毫克,每日三次(n = 15);左旋多巴/卡比多巴25/100毫克,每日三次(n = 15);卡麦角林每周0.5毫克(n = 15);以及每日三次的安慰剂(n = 15),作为可卡因依赖的潜在药物治疗方法。
四平行组的可卡因快速疗效筛选试验(CREST)设计包括一个为期2周的基线期,随后随机分配至为期8周的药物治疗期,其中包括每周1小时的认知行为药物咨询。在试验结束4周后进行安全性评估。
结果包括尿液中测量的可卡因代谢物、药物使用的留存情况和自我报告、对可卡因的渴望、临床改善情况、情绪以及艾滋病毒风险行为。
分配接受卡麦角林治疗的参与者提供的尿液样本中可卡因代谢物呈阴性的比例(42.4%)高于分配接受安慰剂治疗的参与者(25.0%),在控制了自我报告的可卡因使用的基线差异后,这一差异具有统计学意义(F = 2.95,自由度 = 3;P = 0.05)。当使用成瘾严重程度指数(ASI)就业子量表进行测量时,从基线到第8周,接受卡麦角林治疗的参与者相对于安慰剂有显著改善(总体变化 = -0.09,标准差 = 0.10,t = 2.36,P < 0.05)。安全性和不良事件指标显示,不同治疗组的投诉发生率和类型相似。
这些结果,再加上卡麦角林在此人群中使用时明显的安全性,为开展该药物的更大规模研究提供了实证支持。