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纳布西莫尔联合动机增强/认知行为疗法治疗大麻依赖:一项随机临床试验试点研究

Nabiximols combined with motivational enhancement/cognitive behavioral therapy for the treatment of cannabis dependence: A pilot randomized clinical trial.

作者信息

Trigo Jose M, Soliman Alexandra, Quilty Lena C, Fischer Benedikt, Rehm Jürgen, Selby Peter, Barnes Allan J, Huestis Marilyn A, George Tony P, Streiner David L, Staios Gregory, Le Foll Bernard

机构信息

Translational Addiction Research Laboratory, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, Canada.

Campbell Family Mental Health Research Institute, CAMH, Toronto, Canada.

出版信息

PLoS One. 2018 Jan 31;13(1):e0190768. doi: 10.1371/journal.pone.0190768. eCollection 2018.

Abstract

BACKGROUND

The current lack of pharmacological treatments for cannabis use disorder (CUD) warrants novel approaches and further investigation of promising pharmacotherapy. We previously showed that nabiximols (27 mg/ml Δ9-tetrahydrocannabinol (THC)/ 25 mg/ml cannabidiol (CBD), Sativex®) can decrease cannabis withdrawal symptoms. Here, we assessed in a pilot study the tolerability and safety of self-titrated nabiximols vs. placebo among 40 treatment-seeking cannabis-dependent participants.

METHODS

Subjects participated in a double blind randomized clinical trial, with as-needed nabiximols up to 113.4 mg THC/105 mg CBD or placebo daily for 12 weeks, concurrently with Motivational Enhancement Therapy and Cognitive Behavioral Therapy (MET/CBT). Primary outcome measures were tolerability and abstinence, secondary outcome measures were days and amount of cannabis use, withdrawal, and craving scores. Participants received up to CDN$ 855 in compensation for their time.

RESULTS

Medication was well tolerated and no serious adverse events (SAEs) were observed. Rates of adverse events did not differ between treatment arms (F1,39 = 0.205, NS). There was no significant change in abstinence rates at trial end. Participants were not able to differentiate between subjective effects associated with nabiximols or placebo treatments (F1,40 = 0.585, NS). Cannabis use was reduced in the nabiximols (70.5%) and placebo groups (42.6%). Nabiximols reduced cannabis craving but no significant differences between the nabiximols and placebo groups were observed on withdrawal scores.

CONCLUSIONS

Nabiximols in combination with MET/CBT was well tolerated and allowed for reduction of cannabis use. Future clinical trials should explore the potential of high doses of nabiximols for cannabis dependence.

摘要

背景

目前缺乏针对大麻使用障碍(CUD)的药物治疗方法,这使得新方法以及对有前景的药物疗法的进一步研究成为必要。我们之前表明,纳比西莫尔(27毫克/毫升的Δ9 - 四氢大麻酚(THC)/25毫克/毫升的大麻二酚(CBD),商品名Sativex®)可以减轻大麻戒断症状。在此,我们在一项试点研究中评估了40名寻求治疗的大麻依赖参与者中,自我滴定的纳比西莫尔与安慰剂相比的耐受性和安全性。

方法

受试者参与了一项双盲随机临床试验,按需每日服用高达113.4毫克THC/105毫克CBD的纳比西莫尔或安慰剂,持续12周,同时接受动机增强疗法和认知行为疗法(MET/CBT)。主要结局指标是耐受性和戒断情况,次要结局指标是大麻使用的天数和量、戒断症状及渴求分数。参与者因参与研究获得最高855加元的报酬。

结果

药物耐受性良好,未观察到严重不良事件(SAE)。各治疗组之间不良事件发生率无差异(F1,39 = 0.205,无显著性差异)。试验结束时戒断率无显著变化。参与者无法区分与纳比西莫尔或安慰剂治疗相关的主观效应(F1,40 = 0.585,无显著性差异)。纳比西莫尔组(70.5%)和安慰剂组(42.6%)的大麻使用量均有所减少。纳比西莫尔减轻了大麻渴求,但在戒断分数上,纳比西莫尔组与安慰剂组之间未观察到显著差异。

结论

纳比西莫尔联合MET/CBT耐受性良好,且能减少大麻使用。未来的临床试验应探索高剂量纳比西莫尔治疗大麻依赖的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc0f/5791962/c4a24a81fe96/pone.0190768.g001.jpg

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