ADHS
Studienlage · Detail RCT · ADHS · 2017

Cannabinoids in attention-deficit/hyperactivity disorder: A randomised-controlled trial.

Gemischt GRADE Moderat 170 Zitate
Stichproben = 30 Pat.
Dauer17.07.14 to 18.06.15
KontrollePlacebo-Spray
EndpunktQbTest
Verblindungdoppelblind
DesignRCT
Cannabinoidkombination
THC:CBD1:1
Applikationoromukosal
Kernaussage

Keine signifikanten Unterschiede beim primären Outcome (Kognition und Aktivitätslevel), aber nominale Verbesserungen in Sekundär-Outcomes (Hyperaktivität/Impulsivität, Inhibition), die nach Mehrfach-Test-Korrektur die Signifikanz nicht erreichten.

Zusammenfassung

n=30 Erwachsene mit ADHS, randomisiert zu Sativex Oromucosal Spray (n=15) vs. Placebo (n=15). Primäres Outcome (kognitive Leistung/Aktivität via QbTest): kein signifikanter ITT-Unterschied (Est=−0,17, 95% CI −0,40 bis 0,07, p=0,16). Sekundäre Outcomes: nominell signifikante Verbesserung für Hyperaktivität/Impulsivität (p=0,03) und kognitive Inhibition (p=0,05), Trend für Unaufmerksamkeit (p=0,10) und emotionale Labilität (p=0,11). Effekte nicht signifikant nach Multipler-Test-Korrektur. Per-Protokoll-Effekte höher.

P
PopulationErwachsene mit ADHS, n=30
I
InterventionSativex Oromukosal-Spray (THC/CBD-Kombination), orales Spray
C
KontrollePlacebo-Spray
O
OutcomePrimärer Endpunkt (QbTest): kein signifikanter Unterschied (Est=−0,17, 95%-KI −0,40 bis 0,07, p=0,16); nominell signifikante Verbesserung bei Hyperaktivität/Impulsivität (p=0,03) und kognitiver Inhibition (p=0,05)
Vertrauen in die Evidenz
Moderat

Dritte von vier GRADE-Stufen, die Effektschätzung ist wahrscheinlich verlässlich.

Herabgestuft wegen
Ungenauigkeit
Qualitätsprofil
Größe
Verblindung Doppelblind
Effektstärke Gemischt
Zitate / Jahr
Autoren
Cooper RE, Williams E, Seegobin S, Tye C, Kuntsi J, Asherson P
Teilen
Abstract
Adults with ADHD describe self-medicating with cannabis, with some reporting a preference for cannabis over ADHD medications. A small number of psychiatrists in the US prescribe cannabis medication for ADHD, despite there being no evidence from randomised controlled studies. The EMA-C trial (Experimental Medicine in ADHD-Cannabinoids) was a pilot randomised placebo-controlled experimental study of a cannabinoid medication, Sativex Oromucosal Spray, in 30 adults with ADHD. The primary outcome was cognitive performance and activity level using the QbTest. Secondary outcomes included ADHD and emotional lability (EL) symptoms. From 17.07.14 to 18.06.15, 30 participants were randomly assigned to the active (n=15) or placebo (n=15) group. For the primary outcome, no significant difference was found in the ITT analysis although the overall pattern of scores was such that the active group usually had scores that were better than the placebo group (Est=-0.17, 95%CI-0.40 to 0.07, p=0.16, n=15/11 active/placebo). For secondary outcomes Sativex was associated with a nominally significant improvement in hyperactivity/impulsivity (p=0.03) and a cognitive measure of inhibition (p=0.05), and a trend towards improvement for inattention (p=0.10) and EL (p=0.11). Per-protocol effects were higher. Results did not meet significance following adjustment for multiple testing. One serious (muscular seizures/spasms) and three mild adverse events occurred in the active group and one serious (cardiovascular problems) adverse event in the placebo group. Adults with ADHD may represent a subgroup of individuals who experience a reduction of symptoms and no cognitive impairments following cannabinoid use. While not definitive, this study provides preliminary evidence supporting the self-medication theory of cannabis use in ADHD and the need for further studies of the endocannabinoid system in ADHD.

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