Spasticity
Study register · detail Randomized Controlled Trial, Multicenter · Spasticity · 2003

Cannabinoids for treatment of spasticity and other symptoms related to multiple sclerosis (CAMS study): multicentre randomised placebo-controlled trial

Mixed GRADE High 824 citations
Samplen = 630 Pat.
Duration15 weeks
ControlPlacebo, oral
EndpointAshworth scale
Blindingdoppelblind
DesignRandomized Controlled Trial, Multicenter
Cannabinoidkombination
Routeoral
Key finding

No effect on the primary outcome (Ashworth scale for spasticity), but evidence for effects on patient-reported spasticity and pain as well as subjective improvement in mobility.

Summary

n=630 MS patients (33 UK centres, 15 weeks); primary endpoint (Ashworth scale) not met (p=0,40; difference cannabis extract vs. placebo: 0,32, 95% CI –1,04 to 1,67; THC vs. placebo: 0,94, 95% CI –0,44 to 2,31). Secondary, 61 % (cannabis extract), 60 % (THC) and 46 % (placebo) reported a subjective improvement in spasticity (p=0,003); objective improvement in mobility demonstrated.

P
PopulationAdults with stable multiple sclerosis and muscle spasticity, n=630 (ITT: 611)
I
InterventionOral cannabis extract (n=211) or Δ9-THC (n=206), oral, 15 weeks
C
ControlPlacebo (n=213), oral
O
OutcomeNo significant treatment effect on the primary endpoint Ashworth spasticity score (p=0,40); difference cannabis extract vs. placebo: 0,32 (95% CI −1,04 to 1,67), Δ9-THC vs. placebo: 0,94 (95% CI −0,44 to 2,31). Significant effect on patient-reported spasticity and pain (p=0,003).
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
Zajicek J, Fox P, Sanders H et al.
DOI 10.1016/s0140-6736(03)14738-1
Design: Randomized Controlled Trial, Multicenter
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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.

The impediment to action advances action. — Marcus Aurelius