Studienlage · Detail
Gemischt
GRADE
Hoch
824 Zitate
Stichproben = 630 Pat.
Dauer15 Wochen
KontrollePlacebo, oral
EndpunktAshworth-Skala
Verblindungdoppelblind
DesignRandomized Controlled Trial, Multicenter
Cannabinoidkombination
Applikationoral
Kernaussage
Kein Effekt auf das primäre Outcome (Ashworth-Skala für Spastizität), aber Evidenz für Effekte auf patientenberichtete Spastizität und Schmerz sowie subjektive Verbesserung der Mobilität.
Zusammenfassung
n=630 MS-Patienten (33 UK-Zentren, 15 Wochen); primärer Endpunkt (Ashworth-Skala) nicht erreicht (p=0,40; Differenz Cannabis-Extrakt vs. Placebo: 0,32, 95%-KI –1,04 bis 1,67; THC vs. Placebo: 0,94, 95%-KI –0,44 bis 2,31). Sekundär berichteten 61 % (Cannabis-Extrakt), 60 % (THC) und 46 % (Placebo) eine subjektive Spastizitätsverbesserung (p=0,003); objektive Mobilitätsverbesserung nachgewiesen.
P
PopulationErwachsene mit stabiler Multipler Sklerose und Muskelspastizität, n=630 (ITT: 611)
I
InterventionOraler Cannabis-Extrakt (n=211) oder Δ9-THC (n=206), oral, 15 Wochen
C
KontrollePlacebo (n=213), oral
O
OutcomeKein signifikanter Behandlungseffekt auf den primären Endpunkt Ashworth-Spastizitätsscore (p=0,40); Differenz Cannabis-Extrakt vs. Placebo: 0,32 (95% CI −1,04 bis 1,67), Δ9-THC vs. Placebo: 0,94 (95% CI −0,44 bis 2,31). Signifikanter Effekt auf patientenberichtete Spastizität und Schmerzen (p=0,003).
Vertrauen in die Evidenz
Hoch
Höchste von vier GRADE-Stufen, die Effektschätzung ist sehr verlässlich.
Qualitätsprofil
Größe
★★★★★
Verblindung
Doppelblind
Effektstärke
Gemischt
Zitate / Jahr
★★★★★
Autoren
Teilen
Abstract
Multiple sclerosis is associated with muscle stiffness, spasms, pain, and tremor. Much anecdotal evidence suggests that cannabinoids could help these symptoms. Our aim was to test the notion that cannabinoids have a beneficial effect on spasticity and other symptoms related to multiple sclerosis. We did a randomised, placebo-controlled trial, to which we enrolled 667 patients with stable multiple sclerosis and muscle spasticity. 630 participants were treated at 33 UK centres with oral cannabis extract (n=211), Delta9-tetrahydrocannabinol (Delta9-THC; n=206), or placebo (n=213). Trial duration was 15 weeks. Our primary outcome measure was change in overall spasticity scores, using the Ashworth scale. Analysis was by intention to treat. 611 of 630 patients were followed up for the primary endpoint. We noted no treatment effect of cannabinoids on the primary outcome (p=0.40). The estimated difference in mean reduction in total Ashworth score for participants taking cannabis extract compared with placebo was 0.32 (95% CI -1.04 to 1.67), and for those taking Delta9-THC versus placebo it was 0.94 (-0.44 to 2.31). There was evidence of a treatment effect on patient-reported spasticity and pain (p=0.003), with improvement in spasticity reported in 61% (n=121, 95% CI 54.6-68.2), 60% (n=108, 52.5-66.8), and 46% (n=91, 39.0-52.9) of participants on cannabis extract, Delta9-THC, and placebo, respectively. Treatment with cannabinoids did not have a beneficial effect on spasticity when assessed with the Ashworth scale. However, though there was a degree of unmasking among the patients in the active treatment groups, objective improvement in mobility and patients' opinion of an improvement in pain suggest cannabinoids might be clinically useful.
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