Spasticity
Study register · detail Randomized Controlled Trial · Spasticity · 2004

Do cannabis-based medicinal extracts have general or specific effects on symptoms in multiple sclerosis? A double-blind, randomized, placebo-controlled study on 160 patients

Mixed GRADE High 587 citations
Samplen = 160 Pat.
Durationunclear
ControlMatching placebo spray
EndpointVAS
Blindingdoppelblind
DesignRandomized Controlled Trial
Cannabinoidkombination
THC:CBD1:1
Max. dose120.0 mg
Routeoromukosal
Key finding

Primary symptom (VAS) showed no significant difference between CBME and placebo, but spasticity VAS was reduced significantly more by CBME than placebo (P=0,001).

Summary

Multicenter RCT (n=160, MS patients with spasticity among other symptoms); CBME (THC/CBD, Sativex precursor) vs. placebo; spasticity VAS significantly reduced (p=0,001); primary overall symptom score n.s.; no cognitive side effects or relevant intoxication.

P
PopulationAdults with multiple sclerosis (MS) and significant symptoms (spasticity, spasms, bladder problems, tremor or pain), n=160, outpatients from three centers
I
InterventionOromucosal spray with whole-plant CBME (THC:CBD 1:1, 2,5–120 mg/day each in single doses; Sativex)
C
ControlMatching placebo spray (oromucosal)
O
OutcomePrimary endpoint (VAS for the individually most troublesome symptom): reduction from 74,36 to 48,89 (CBME) vs. 74,31 to 54,79 (placebo), not significant. Spasticity VAS significantly reduced by CBME vs. placebo (p=0,001).
Confidence in the evidence
High

The highest of four GRADE levels, the effect estimate is very reliable.

Quality profile
Sample size
Blinding Double-blind
Effect size Mixed
Citations / year
Authors
Wade D T, Makela P, Robson P et al.
DOI 10.1191/1352458504ms1082oa
Design: Randomized Controlled Trial
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Abstract
The objective was to determine whether a cannabis-based medicinal extract (CBME) benefits a range of symptoms due to multiple sclerosis (MS). A parallel group, double-blind, randomized, placebo-controlled study was undertaken in three centres, recruiting 160 outpatients with MS experiencing significant problems from at least one of the following: spasticity, spasms, bladder problems, tremor or pain. The interventions were oromucosal sprays of matched placebo, or whole plant CBME containing equal amounts of delta-9-tetrahydrocannabinol (THC) and cannabidiol (CBD) at a dose of 2.5-120 mg of each daily, in divided doses. The primary outcome measure was a Visual Analogue Scale (VAS) score for each patient's most troublesome symptom. Additional measures included VAS scores of other symptoms, and measures of disability, cognition, mood, sleep and fatigue. Following CBME the primary symptom score reduced from mean (SE) 74.36 (11.1) to 48.89 (22.0) following CBME and from 74.31 (12.5) to 54.79 (26.3) following placebo [ns]. Spasticity VAS scores were significantly reduced by CBME (Sativex) in comparison with placebo (P =0.001). There were no significant adverse effects on cognition or mood and intoxication was generally mild.

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