Studienlage · Detail
Gemischt
GRADE
Hoch
225 Zitate
Stichproben = 156 Pat.
Dauer12 Wochen
KontrollePlacebo
EndpunktAbstinenzrate
Verblindungdoppelblind
DesignRCT (randomisiert, doppelblind, placebo-kontrolliert)
Cannabinoidthc
Max. Dosis40.0 mg
Applikationoral
Kernaussage
Dronabinol steigerte die Therapieretention und reduzierte Entzugssymptome, zeigte jedoch keinen signifikanten Effekt auf Cannabis-Abstinenz gegenüber Placebo.
Zusammenfassung
n=156 cannabis-abhängige Erwachsene, 12-Wochen-DB-RCT Dronabinol 20 mg 2×/Tag vs. Placebo; primärer Endpunkt Abstinenz nicht signifikant (Dronabinol 17,7% vs. Placebo 15,6%); Therapieverbleib signifikant höher unter Dronabinol (77% vs. 61%, p=0,02); Entzugssymptome signifikant geringer (p=0,02).
P
PopulationErwachsene mit Cannabis-Abhängigkeit, n=156
I
InterventionDronabinol 20 mg zweimal täglich oral, 8 Wochen Erhaltung + 2 Wochen Ausschleichen
C
KontrollePlacebo (identisches orales Präparat)
O
OutcomeKein signifikanter Unterschied in der 2-Wochen-Abstinenzrate am Ende der Erhaltungsphase (Dronabinol: 17,7% vs. Placebo: 15,6%); signifikant höhere Therapieretention unter Dronabinol (77% vs. 61%, p=0,02) und signifikant geringere Entzugssymptome (p=0,02)
Vertrauen in die Evidenz
Hoch
Höchste von vier GRADE-Stufen, die Effektschätzung ist sehr verlässlich.
Qualitätsprofil
Größe
★★★★★
Verblindung
Doppelblind
Effektstärke
Gemischt
Zitate / Jahr
★★★★★
Autoren
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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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