Chronic Pain
Study register · detail RCT (crossover, 3-armig) · Chronic Pain · 2004

Efficacy of two cannabis based medicinal extracts for relief of central neuropathic pain from brachial plexus avulsion: results of a randomised controlled trial

Mixed GRADE Moderate 361 citations
Samplen = 48 Pat.
Duration2 weeks baseline + three 2-week…
ControlPlacebo spray
EndpointMean pain severity score
Blindingdoppelblind
DesignRCT (crossover, 3-armig)
Cannabinoidkombination
THC:CBD1:1
Routeoromukosal
Key finding

Statistically significant improvement in pain and sleep, but without reaching the clinically relevant minimum reduction.

Summary

n=48 patients with treatment-refractory chronic neuropathic pain (brachial plexus avulsion), Sativex vs. THC vs. placebo (2-week treatment periods); pain severity scores showed statistically significant improvement despite the primary endpoint (reduction >2 points) not being reached. Cannabis extracts well tolerated; AEs mild to moderate.

P
PopulationAdults with chronic central neuropathic pain following brachial plexus avulsion, n=48, pain score ≥4 on 11-point scale
I
InterventionOromucosal sprays: GW-1000-02 (Sativex, THC:CBD ≈1:1) and GW-2000-02 (primarily THC), each for 2 weeks
C
ControlPlacebo spray (oromucosal)
O
OutcomePrimary endpoint (mean pain score over last 7 days) missed the predefined reduction of 2 points; however, statistically significant improvements in pain and sleep
Confidence in the evidence
Moderate

The third of four GRADE levels, the effect estimate is probably reliable.

Downgraded for
Imprecision
Quality profile
Sample size
Blinding Double-blind
Effect size Mixed
Citations / year
Authors
Berman J S, Symonds C, Birch R
DOI 10.1016/j.pain.2004.09.013
Design: RCT (crossover, 3-armig)
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Abstract
The objective was to investigate the effectiveness of cannabis-based medicines for treatment of chronic pain associated with brachial plexus root avulsion. This condition is an excellent human model of central neuropathic pain as it represents an unusually homogenous group in terms of anatomical location of injury, pain descriptions and patient demographics. Forty-eight patients with at least one avulsed root and baseline pain score of four or more on an 11-point ordinate scale participated in a randomised, double-blind, placebo-controlled, three period crossover study. All patients had intractable symptoms regardless of current analgesic therapy. Patients entered a baseline period of 2 weeks, followed by three, 2-week treatment periods during each of which they received one of three oromucosal spray preparations. These were placebo and two whole plant extracts of Cannabis sativa L.: GW-1000-02 (Sativex), containing Delta(9)tetrahydrocannabinol (THC):cannabidiol (CBD) in an approximate 1:1 ratio and GW-2000-02, containing primarily THC. The primary outcome measure was the mean pain severity score during the last 7 days of treatment. Secondary outcome measures included pain related quality of life assessments. The primary outcome measure failed to fall by the two points defined in our hypothesis. However, both this measure and measures of sleep showed statistically significant improvements. The study medications were generally well tolerated with the majority of adverse events, including intoxication type reactions, being mild to moderate in severity and resolving spontaneously. Studies of longer duration in neuropathic pain are required to confirm a clinically relevant, improvement in the treatment of this condition.

The impediment to action advances action. — Marcus Aurelius