Cannabis use in patients 3 months after ceasing nabiximols for the treatment of cannabis dependence: Results from a placebo-controlled randomised trial

•Cannabinoid medications hold promise in treating cannabis dependence, but outcomes post-treatment are unclear.•We examine outcomes after a 12-week RCT comparing nabiximols (containing equal parts THC & CBD) v placebo.•The nabiximols group reported less cannabis use 12 weeks after stopping treat...

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Veröffentlicht in:Drug and alcohol dependence 2020-10, Vol.215, p.108220, Article 108220
Hauptverfasser: Lintzeris, Nicholas, Mills, Llewellyn, Dunlop, Adrian, Copeland, Jan, Mcgregor, Iain, Bruno, Raimondo, Kirby, Adrienne, Montebello, Mark, Hall, Michelle, Jefferies, Meryem, Kevin, Richard, Bhardwaj, Anjali
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container_issue
container_start_page 108220
container_title Drug and alcohol dependence
container_volume 215
creator Lintzeris, Nicholas
Mills, Llewellyn
Dunlop, Adrian
Copeland, Jan
Mcgregor, Iain
Bruno, Raimondo
Kirby, Adrienne
Montebello, Mark
Hall, Michelle
Jefferies, Meryem
Kevin, Richard
Bhardwaj, Anjali
description •Cannabinoid medications hold promise in treating cannabis dependence, but outcomes post-treatment are unclear.•We examine outcomes after a 12-week RCT comparing nabiximols (containing equal parts THC & CBD) v placebo.•The nabiximols group reported less cannabis use 12 weeks after stopping treatment.•A 12-week intervention of counselling with nabiximols is suggested. Previous studies suggest cannabinoid agonist treatment is effective in reducing cannabis use in dependent treatment seekers, however few studies have reported on post-treatment outcomes. We examine cannabis use outcomes 12 weeks after cessation of treatment from a randomised placebo-controlled trial of nabiximols for the treatment of cannabis dependence. 128 participants received either nabiximols (n = 61) or placebo (n = 67) for 12 weeks, in combination with psychosocial interventions. Self-reported number of days of cannabis use in the previous 28 days was measured at baseline, 4, 8, and 12 weeks (end of treatment) and again at 24 weeks (3 months after treatment ceased). Urinalysis was used to confirm self-report data at Week 24 interview. A factorial mixed-effects model for repeated measures regression revealed that the nabiximols group used cannabis on 6.8 fewer days in the previous 28 days at week 12 (end of treatment) than the placebo group (p = 0.002, CI: 2.1,11.4), and 6.7 fewer days in the previous 28 days at the week-24 follow-up than the placebo group (p = 0.006, CI: 1.4,12.1). A significantly higher proportion of the nabiximols group (14/61; 23 %) than the placebo group (6/67; 9%) reported abstinence from cannabis in the previous 28 days at the week-24 research interview OR=3.0, CI: 1.1, 9.1; p=0.035, NNT=8, CI: 4, 71). The benefits of treatment incorporating nabiximols with psychosocial interventions in reducing cannabis use appears to persist for up to 3 months after the cessation of treatment. A stepped care model of treatment is proposed. Australian New Zealand Clinical Trials Registry (ACTRN12616000103460) https://www.anzctr.org.au
doi_str_mv 10.1016/j.drugalcdep.2020.108220
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(Arc-D) ; Agonist Replacement For Cannabis Dependence Study Group. (Arc-D)</creatorcontrib><description>•Cannabinoid medications hold promise in treating cannabis dependence, but outcomes post-treatment are unclear.•We examine outcomes after a 12-week RCT comparing nabiximols (containing equal parts THC &amp; CBD) v placebo.•The nabiximols group reported less cannabis use 12 weeks after stopping treatment.•A 12-week intervention of counselling with nabiximols is suggested. Previous studies suggest cannabinoid agonist treatment is effective in reducing cannabis use in dependent treatment seekers, however few studies have reported on post-treatment outcomes. We examine cannabis use outcomes 12 weeks after cessation of treatment from a randomised placebo-controlled trial of nabiximols for the treatment of cannabis dependence. 128 participants received either nabiximols (n = 61) or placebo (n = 67) for 12 weeks, in combination with psychosocial interventions. Self-reported number of days of cannabis use in the previous 28 days was measured at baseline, 4, 8, and 12 weeks (end of treatment) and again at 24 weeks (3 months after treatment ceased). Urinalysis was used to confirm self-report data at Week 24 interview. A factorial mixed-effects model for repeated measures regression revealed that the nabiximols group used cannabis on 6.8 fewer days in the previous 28 days at week 12 (end of treatment) than the placebo group (p = 0.002, CI: 2.1,11.4), and 6.7 fewer days in the previous 28 days at the week-24 follow-up than the placebo group (p = 0.006, CI: 1.4,12.1). A significantly higher proportion of the nabiximols group (14/61; 23 %) than the placebo group (6/67; 9%) reported abstinence from cannabis in the previous 28 days at the week-24 research interview OR=3.0, CI: 1.1, 9.1; p=0.035, NNT=8, CI: 4, 71). The benefits of treatment incorporating nabiximols with psychosocial interventions in reducing cannabis use appears to persist for up to 3 months after the cessation of treatment. A stepped care model of treatment is proposed. 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(Arc-D)</creatorcontrib><creatorcontrib>Agonist Replacement For Cannabis Dependence Study Group. (Arc-D)</creatorcontrib><title>Cannabis use in patients 3 months after ceasing nabiximols for the treatment of cannabis dependence: Results from a placebo-controlled randomised trial</title><title>Drug and alcohol dependence</title><addtitle>Drug Alcohol Depend</addtitle><description>•Cannabinoid medications hold promise in treating cannabis dependence, but outcomes post-treatment are unclear.•We examine outcomes after a 12-week RCT comparing nabiximols (containing equal parts THC &amp; CBD) v placebo.•The nabiximols group reported less cannabis use 12 weeks after stopping treatment.•A 12-week intervention of counselling with nabiximols is suggested. Previous studies suggest cannabinoid agonist treatment is effective in reducing cannabis use in dependent treatment seekers, however few studies have reported on post-treatment outcomes. We examine cannabis use outcomes 12 weeks after cessation of treatment from a randomised placebo-controlled trial of nabiximols for the treatment of cannabis dependence. 128 participants received either nabiximols (n = 61) or placebo (n = 67) for 12 weeks, in combination with psychosocial interventions. Self-reported number of days of cannabis use in the previous 28 days was measured at baseline, 4, 8, and 12 weeks (end of treatment) and again at 24 weeks (3 months after treatment ceased). Urinalysis was used to confirm self-report data at Week 24 interview. A factorial mixed-effects model for repeated measures regression revealed that the nabiximols group used cannabis on 6.8 fewer days in the previous 28 days at week 12 (end of treatment) than the placebo group (p = 0.002, CI: 2.1,11.4), and 6.7 fewer days in the previous 28 days at the week-24 follow-up than the placebo group (p = 0.006, CI: 1.4,12.1). 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subjects Australia
Cannabidiol
Cannabinoid Receptor Agonists - therapeutic use
Cannabinoid receptors
Cannabis
Clinical outcomes
Dependence
Diagnostic tests
Dronabinol
Drug Combinations
Female
Health services utilization
Help seeking behavior
Humans
Interviews
Male
Marijuana
Marijuana Abuse - therapy
Marijuana Smoking
Nabiximols
Outcomes
Psychosocial factors
Psychosocial intervention
Psychosocial therapy
RCT
Regression models
Self report
Substance-Related Disorders
Treatment
Treatment Outcome
Urinalysis
title Cannabis use in patients 3 months after ceasing nabiximols for the treatment of cannabis dependence: Results from a placebo-controlled randomised trial
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