Multiple Sklerose
Studienlage · Detail RCT (randomized, double-blind, placebo-controlled crossover) · Multiple Sklerose · 2004

Efficacy, safety and tolerability of an orally administered cannabis extract in the treatment of spasticity in patients with multiple sclerosis: a randomized, double-blind, placebo-controlled, crossover study

Gemischt GRADE Moderat 262 Zitate
Stichproben = 50 Pat.
Dauer14 Tage aktive Behandlung, 7…
KontrollePlacebo-Kapseln
EndpunktAshworth Scale
Verblindungdoppelblind
DesignRCT (randomized, double-blind, placebo-controlled crossover)
Cannabinoidkombination
THC:CBD2.78:1
Max. Dosis30.0 mg
Applikationoral
Kernaussage

Im Per-Protocol-Kollektiv signifikante Verbesserung der Spasmusfrequenz und Mobilität, im ITT-Set jedoch keine statistisch signifikanten Effekte.

Zusammenfassung

n=50 MS-Patienten mit schlecht kontrollierter Spastik (ITT-Analyse); Cannabis-sativa-Extrakt vs. Placebo; Per-Protocol (n=37): signifikante Spasmusfrequenzreduktion (p=0,013) und Mobilitätsverbesserung (p=0,01); ITT-Analyse zeigt nur Trends. Verträglichkeit gut; leichte UAW während der Wirkstoffphase häufiger.

P
PopulationMS-Patienten mit schlecht kontrollierter Spastik während stationärer Rehabilitation, n=57 (ITT: n=50, Per-Protocol: n=37)
I
InterventionOrales Cannabis-Extrakt (Kapseln), standardisiert auf 2,5 mg THC + 0,9 mg CBD pro Kapsel, Dosistitration 15–30 mg THC/Tag über 14 Tage
C
KontrollePlacebo-Kapseln (doppelblind, Crossover)
O
OutcomeIm ITT-Set keine signifikanten Unterschiede; im Per-Protocol-Set signifikante Reduktion der Spasmusfrequenz (p=0,013) und verbesserte Mobilität (p=0,01) unter aktiver Behandlung vs. Placebo
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
Vaney C, Heinzel-Gutenbrunner M, Jobin P et al.
DOI 10.1191/1352458504ms1048oa
Design: RCT (randomized, double-blind, placebo-controlled crossover)
Teilen
Abstract
<h4>Objective</h4>Cannabis may alleviate some symptoms associated with multiple sclerosis (MS). This study investigated the effect of an orally administered standardized Cannabis sativa plant extract in MS patients with poorly controlled spasticity.<h4>Methods</h4>During their inpatient rehabilitation programme, 57 patients were enrolled in a prospective, randomized, double-blind, placebo-controlled crossover study of cannabis-extract capsules standardized to 2.5 mg tetrahydrocannabinol (THC) and 0.9 mg cannabidiol (CBD) each. Patients in group A started with a drug escalation phase from 15 to maximally 30 mg THC by 5 mg per day if well tolerated, being on active medication for 14 days before starting placebo. Patients in group B started with placebo for seven days, crossed to the active period (14 days) and closed with a three-day placebo period (active drug dose escalation and placebo sham escalation as in group A). Measures used included daily self-report of spasm frequency and symptoms, Ashworth Scale, Rivermead Mobility Index, 10-m timed walk, nine-hole peg test, paced auditory serial addition test (PASAT), and the digit span test.<h4>Results</h4>In the 50 patients included into the intention-to-treat analysis set, there were no statistically significant differences associated with active treatment compared to placebo, but trends in favour of active treatment were seen for spasm frequency, mobility and getting to sleep. In the 37 patients (per-protocol set) who received at least 90% of their prescribed dose, improvements in spasm frequency (P = 0.013) and mobility after excluding a patient who fell and stopped walking were seen (P = 0.01). Minor adverse events were slightly more frequent and severe during active treatment, and toxicity symptoms, which were generally mild, were more pronounced in the active phase.<h4>Conclusion</h4>A standardized Cannabis sativa plant extract might lower spasm frequency and increase mobility with tolerable side effects in MS patients with persistent spasticity not responding to other drugs.

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