Study register · detail
Mixed
GRADE
High
225 citations
Samplen = 156 Pat.
Duration12 weeks
ControlPlacebo
EndpointAbstinence rate
Blindingdoppelblind
DesignRCT (randomisiert, doppelblind, placebo-kontrolliert)
Cannabinoidthc
Max. dose40.0 mg
Routeoral
Key finding
Dronabinol increased treatment retention and reduced withdrawal symptoms, but showed no significant effect on cannabis abstinence versus placebo.
Summary
n=156 cannabis-dependent adults, 12-week DB-RCT dronabinol 20 mg 2×/day vs. placebo; primary endpoint abstinence not significant (dronabinol 17,7% vs. placebo 15,6%); treatment retention significantly higher under dronabinol (77% vs. 61%, p=0,02); withdrawal symptoms significantly lower (p=0,02).
P
PopulationAdults with cannabis dependence, n=156
I
InterventionDronabinol 20 mg twice daily orally, 8 weeks maintenance + 2 weeks taper
C
ControlPlacebo (identical oral preparation)
O
OutcomeNo significant difference in the 2-week abstinence rate at the end of the maintenance phase (dronabinol: 17,7% vs. placebo: 15,6%); significantly higher treatment retention under dronabinol (77% vs. 61%, p=0,02) and significantly lower withdrawal symptoms (p=0,02)
Confidence in the evidence
High
The highest of four GRADE levels, the effect estimate is very reliable.
Quality profile
Sample size
★★★★★
Blinding
Double-blind
Effect size
Mixed
Citations / year
★★★★★
Authors
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Abstract
Cannabis dependence is a substantial public health problem. Behavioral treatments have shown promise, but there are no effective medications for cannabis dependence. The purpose of this study was to evaluate the safety and efficacy of dronabinol, a synthetic form of delta-9-tetrahydrocannabinol, a naturally occurring pharmacologically active component of Cannabis, in treating cannabis dependence. 156 cannabis-dependent adults were enrolled in a randomized, double-blind, placebo-controlled, 12-week trial. After a 1-week placebo lead-in phase, participants were randomized to receive dronabinol 20mg twice a day or placebo. Doses were maintained until the end of week 8 and then tapered off over 2 weeks. All participants received weekly motivational enhancement and relapse prevention therapy. Cannabis use was assessed using the timeline follow back method. There was no significant difference between treatment groups in the proportion of participants who achieved 2 weeks of abstinence at the end of the maintenance phase (dronabinol: 17.7%; placebo: 15.6%). Although both groups showed a reduction in Cannabis use over time, there were no differences between the groups. Treatment retention was significantly higher at the end of the maintenance phase on dronabinol (77%), compared to placebo (61%) (P=.02), and withdrawal symptoms were significantly lower on dronabinol than placebo (P=.02). This is the first trial using an agonist substitution strategy for treatment of cannabis dependence. Dronabinol showed promise, it was well-tolerated, and improved treatment retention and withdrawal symptoms. Future trials might test higher doses, combinations of dronabinol with other medications with complementary mechanisms, or with more potent behavioral interventions.
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