Spasticity
Study register · detail Kohortenstudie · Spasticity · 2015

Drug-resistant MS spasticity treatment with Sativex((R)) add-on and driving ability.

Clear benefit GRADE Very low 36 citations
Samplen = 33 Pat.
Duration4-6 weeks
EndpointFitness to drive
Blindingn.a.
DesignKohortenstudie
Cannabinoidkombination
THC:CBD1:1
Routeoromukosal
Key finding

Sativex does not negatively affect fitness to drive and statistically significantly improves self-reported spasticity severity.

Summary

n=33 MS patients with treatment-resistant spasticity, 4-6 weeks Sativex add-on therapy. Fitness-to-drive tests (validated computer-based test battery) showed no deterioration under treatment; only 2 patients changed classification (1 to 'fit', 1 to 'unfit'). Mean spasticity severity (self-report) improved statistically significantly (p<0.05). Sativex well tolerated.

P
PopulationMS patients with moderate to severe treatment-resistant spasticity, n=33
I
InterventionSativex (THC/CBD oromucosal spray) as add-on therapy over 4–6 weeks
O
OutcomeFitness to drive (computerised test battery) remained unchanged under Sativex therapy; spasticity severity improved statistically significantly
Confidence in the evidence
Very low

The lowest GRADE level, the effect estimate remains uncertain.

Downgraded for
Imprecision
Quality profile
Sample size
Blinding
Effect size Clear benefit
Citations / year
Authors
Freidel M, Tiel-Wilck K, Schreiber H, Prechtl A, Essner U, Lang M
DOI 10.1111/ane.12287
Design: Kohortenstudie
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Abstract
Objective: The aim of the present observational study was to determine the effects of a delta-9-tetrahydrocannabinol (THC) and cannabidiol (CBD) oromucosal spray (Sativex((R)) spray), brand name Sativex((R)), indicated for drug-resistant MS spasticity, on the driving ability of treated MS patients. Methods: The study was conducted over a period of 4-6 weeks. Thirty-three MS patients with moderate to severe treatment-resistant spasticity and planned to begin add-on treatment with Sativex((R)) were enrolled at three specialized MS centres in Germany. A set of five driving test procedures from a validated computerized test battery was used to evaluate the driving ability of eligible patients. Tests were performed by patients at baseline and repeated after 4-6 weeks of treatment with Sativex((R)) oromucosal spray. According to German normative data, the test thresholds achieved by the general population served as a reference to allow for a fitness/unfitness to drive classification. Results: Patients showed comparable driving test results at baseline and at final visits. Only two patients changed classification shifting from 'unfit' to drive to 'fit' and vice versa. The mean severity of spasticity, as self-reported by the patients, improved with statistical significance. Sativex((R)) was generally well tolerated. Conclusions: Treatment of MS patients with Sativex((R)) does not negatively impact on driving ability and may improve moderate to severe treatment-resistant MS spasticity.

The impediment to action advances action. — Marcus Aurelius