Multiple Sclerosis
Study register · detail RCT · Multiple Sclerosis · 2012

MUltiple Sclerosis and Extract of Cannabis: results of the MUSEC trial

Clear benefit GRADE High 0 citations
Samplen = 279 Pat.
Duration2 weeks titration + 10 weeks…
ControlPlacebo
EndpointCRS
Blindingdoppelblind
DesignRCT
Cannabinoidvollspektrum
Max. dose25.0 mg
Routeoral
Key finding

Cannabis extract showed almost twice the muscle stiffness relief compared with placebo (29,4% vs. 15,7%; p=0,004).

Summary

MUSEC trial: multicentre phase III RCT (n=279, 22 UK centres) of oral cannabis extract vs. placebo in stable MS over 12 weeks (2 weeks titration 5-25 mg THC daily, 10 weeks maintenance). Primary endpoint muscle stiffness: response rate cannabis 29,4% vs. placebo 15,7% (OR=2,26; 95% CI: 1,24-4,13; p=0,004 one-sided) — nearly double the success rate. Comparable effects at 4 and 8 weeks; secondary endpoints (pain, spasms, sleep quality) support the primary finding. Adverse effects consistent with the known cannabinoid profile.

P
PopulationAdults with stable multiple sclerosis, n=279 (CE n=144, placebo n=135)
I
InterventionOral cannabis extract (CE), dose titration 5–25 mg THC/day over 2 weeks, followed by a 10-week maintenance phase
C
ControlPlacebo (oral, identical schedule)
O
OutcomeRate of relief of muscle stiffness after 12 weeks: 29,4% (CE) vs. 15,7% (placebo); OR 2,26 (95% CI 1,24–4,13; p=0,004, one-sided)
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 Clear benefit
Citations / year
Authors
Zajicek JP, Hobart JC, Slade A et al
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Abstract
Objective: Multiple sclerosis (MS) is associated with chronic symptoms, including muscle stiffness, spasms, pain and insomnia. Here we report the results of the Multiple Sclerosis and Extract of Cannabis (MUSEC) study that aimed to substantiate the patient based findings of previous studies. Patients And Methods: Patients with stable MS at 22 UK centres were randomised to oral cannabis extract (CE) (N=144) or placebo (N=135), stratified by centre, walking ability and use of antispastic medication. This double blind, placebo controlled, phase III study had a screening period, a 2 week dose titration phase from 5 mg to a maximum of 25 mg of tetrahydrocannabinol daily and a 10 week maintenance phase. The primary outcome measure was a category rating scale (CRS) measuring patient reported change in muscle stiffness from baseline. Further CRSs assessed body pain, spasms and sleep quality. Three validated MS specific patient reported outcome measures assessed aspects of spasticity, physical and psychological impact, and walking ability. Results: The rate of relief from muscle stiffness after 12 weeks was almost twice as high with CE than with placebo (29.4% vs. 15.7%; OR 2.26; 95% CI 1.24 to 4.13; p=0.004, one sided). Similar results were found after 4 weeks and 8 weeks, and also for all further CRSs. Results from the MS scales supported these findings. Conclusion: The study met its primary objective to demonstrate the superiority of CE over placebo in the treatment of muscle stiffness in MS. This was supported by results for secondary efficacy variables. Adverse events in participants treated with CE were consistent with the known side effects of cannabinoids. No new safety concerns were observed. Trial Registration Number: NCT00552604.

The impediment to action advances action. — Marcus Aurelius