Studienlage · Detail
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GRADE
Hoch
27 Zitate
Stichproben = 134 Pat.
Dauer6 Wochen Behandlung, 1 Woche…
KontrollePlacebo, 6 Wochen
EndpunktNRS
Verblindungdoppelblind
DesignRCT (parallel, 4-arm)
Cannabinoidkombination
Max. Dosis67.5 mg
Applikationoral
Kernaussage
THC, CBD und deren Kombination reduzierten neuropathischen Schmerz und Spastik nicht signifikant gegenüber Placebo.
Zusammenfassung
Randomisierte, doppelblinde, placebokontrollierte 4-Arm-Studie (n=134; MS n=119, SCI n=15): THC, CBD, THC+CBD vs. Placebo über 6 Wochen bei zentralem neuropathischem Schmerz und/oder Spastik. Kein signifikanter Unterschied beim mittleren Schmerzintensitäts-Score (THC: Δ0,42 [95% CI −0,54 bis 1,38]; CBD: Δ0,45 [−0,47 bis 1,38]; THC+CBD: Δ0,16 [−0,75 bis 1,08]) gegenüber Placebo. Auch für Spastik und sekundäre Outcomes kein Effekt nachweisbar.
P
PopulationErwachsene mit MS oder Rückenmarksverletzung und zentralem neuropathischem Schmerz (NRS >3–≤9) und/oder Spastik (NRS >3), n=134 (MS n=119, SCI n=15)
I
InterventionTHC (max. 22,5 mg/Tag), CBD (max. 45 mg/Tag) oder THC+CBD (max. 22,5/45 mg/Tag), oral, 6 Wochen
C
KontrollePlacebo, 6 Wochen
O
OutcomeKein signifikanter Unterschied in der mittleren Schmerzintensität (THC: 0,42; CBD: 0,45; THC+CBD: 0,16 vs. Placebo) oder Spastikintensität (THC: 0,24; CBD: 0,46; THC+CBD: 0,10 vs. Placebo); alle 95%-KI schließen Null ein
Vertrauen in die Evidenz
Hoch
Höchste von vier GRADE-Stufen, die Effektschätzung ist sehr verlässlich.
Qualitätsprofil
Größe
★★★★★
Verblindung
Doppelblind
Effektstärke
Kein Nutzen
Zitate / Jahr
★★★★★
Autoren
Teilen
Abstract
Patients with multiple sclerosis (MS) and spinal cord injury (SCI) commonly sustain central neuropathic pain (NP) and spasticity. Despite a lack of consistent evidence, cannabis-based medicine (CBM) has been suggested as a supplement treatment. We aimed to investigate the effect of CBM on NP and spasticity in patients with MS or SCI. We performed a randomized, double-blinded, placebo-controlled trial in Denmark. Patients aged ≥18 years with NP (intensity >3, ≤9 on a numerical rating scale (NRS0-10) and/or spasticity (>3 on NRS0-10) were randomized to treatment consisting of either delta-9-tetrahydrocannabinol (THC), cannabidiol (CBD), a combination of THC&CBD in maximum doses of 22.5 mg, 45 mg and 22.5/45 mg per day, respectively, or placebo. A baseline registration was performed before randomization. Treatment duration was six weeks followed by a one-week phaseout. Primary endpoints were the intensity of patient-reported NP and/or spasticity. Between February 2019 and December 2021, 134 patients were randomized (MS <i>n</i> = 119, SCI <i>n</i> = 15), where 32 were assigned to THC, 31 to CBD, 31 to THC&CBD, and 40 to placebo. No significant difference was found for: mean pain intensity (THC 0.42 (-0.54-1.38), CBD 0.45 (-0.47-1.38) and THC&CBD 0.16 (-0.75-1.08)), mean spasticity intensity (THC 0.24 (-0.67-1.45), CBD 0.46 (-0.74-1.65), and THC&CBD 0.10 (-1.18-1.39), secondary outcomes (patient global impression of change and quality of life), or any tertiary outcomes. We aimed to include 448 patients in the trial; however, due to COVID-19 and recruitment challenges, fewer were included. Nevertheless, in this four-arm parallel trial, no effect was found between placebo and active treatment with THC or CBD alone or in combination on NP or spasticity in patients with either MS or SCI. The trial was registered with the EU Clinical Trials Register EudraCT (2018-002315-98).
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