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Journal of Clinical and
            Translational Research                                               Cannabinoids for cannabis use disorder
























































                                        Figure 1. PRISMA flow diagram of study screening and selection

              The studies used five different CB preparations as   3.3. Study outcomes
            interventions: nabiximols (n = 3), CBD (n = 1), nabilone   3.3.1. Cannabis use
            (n = 1), dronabinol (n = 1), and a combination of
            dronabinol and lofexidine (n = 1). All participants received   Nabiximols significantly reduced self-reported cannabis use
            supplementary psychosocial therapy during the active   compared to placebo in 3 studies 19,23,24  and had no significant
            treatment period in all trials.                    effect in another study. Treatments of daily CBD 400 mg and
              The treatment duration ranged from 9 to 84  days.   800 mg showed greater effectiveness in reducing cannabis
            One study was conducted within a 4-week assessment   use over a 30-day treatment period compared to a placebo, as
            interval 17,18,20  and five studies had an assessment frequency   evidenced by a decrease in urinary THC-COOH: creatinine
            of  1  –  2  times  per  week. 17-20,22   One  study  included  an   ratios²². However, the 400  mg dose decreased THC-
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            inpatient treatment phase of up to 9 days.  Two studies had   COOH:  creatinine ratio by 94.21  ng/mL, whereas the
            a follow-up assessment after 28 days, 18,21  one trial included   800 mg dose decreased by 72.02 ng/mL, suggesting that the
            multiple follow-up assessments up to 168 days,  and one   400mg dose might be slightly more effective²². Nabilone and
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            study conducted follow-up 84 days after treatment.  The   dronabinol did not affect the magnitude of cannabis use
                                                     24
            study characteristics are summarized in Table 1.   compared to placebo. 18,20

            Volume 11 Issue 1 (2025)                        7                             doi: 10.36922/jctr.24.00066
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