Study register · detail
Clear benefit
GRADE
Moderate
121 citations
Samplen = 15 Pat.
Duration9 weeks, 63-day follow-up
ControlPlacebo oral as adjunct to gabapentin
EndpointVAS
Blindingdoppelblind
DesignRCT (doppelblind, placebokontrolliert)
Cannabinoidthc
Max. dose2.0 mg
Routeoral
Key finding
Nabilone as add-on therapy to gabapentin showed a statistically significantly greater reduction in pain intensity (VASpain) and impact on daily activities (VASimpact) compared to placebo (both P < 0,01).
Summary
n=15 MS patients with neuropathic pain on gabapentin (≥1.800 mg/day), nabilone (1 mg 2×/day) as add-on vs. placebo over 9 weeks (4 weeks titration + 5 weeks maintenance); significantly greater decrease in VASpain (p<0.01) and VASimpact (p<0.01) with nabilone after adjustment for covariates. Nabilone well tolerated, most common side effects dizziness/drowsiness.
P
PopulationAdults with relapsing-remitting MS and MS-induced neuropathic pain, stable on gabapentin ≥1.800 mg/day, n=15
I
InterventionNabilone oral 1 mg twice daily (titration over 4 weeks, then 5 weeks maintenance) as adjunct to gabapentin
C
ControlPlacebo oral (identical schedule) as adjunct to gabapentin
O
OutcomeSignificantly greater decrease in VASpain and VASimpact in the nabilone group vs. placebo (group × time² interaction, p<0,01 for both outcomes)
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
Clear benefit
Citations / year
★★★★★
Authors
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Abstract
Background: Neuropathic pain (NPP) is a chronic syndrome suffered by patients with multiple sclerosis (MS), for which there is no cure. Underlying cellular mechanisms involved in its pathogenesis are multifaceted, presenting significant challenges in its management.
Methods: A randomized, double-blind, placebo-controlled study involving 15 relapsing-remitting MS patients with MS-induced NPP was conducted to evaluate nabilone combined with gabapentin (GBP). Eligible patients stabilized on GBP (>/=1,800 mg/day) with inadequate pain relief were recruited. Nabilone or placebo was titrated over 4 weeks (0.5 mg/week increase) followed by 5-week maintenance of 1 mg oral nabilone (placebo) twice daily. Primary outcomes included two daily patient-reported measures using a 100-mm visual analog scale (VAS), pain intensity (VASpain), and impact of pain on daily activities (VASimpact). Hierarchical regression modeling was conducted on each outcome to determine if within-person pain trajectory differed across study groups, during 63-day follow-up.
Results: After adjustment for key patient-level covariates (e.g., age, sex, Expanded Disability Status Scale, duration of MS, baseline pain), a significant group x time(2) interaction term was reported for both the VASpain (P < 0.01) and VASimpact score (P < 0.01), demonstrating the adjusted rate of decrease for both outcomes was statistically greater in nabilone vs placebo study group. No significant difference in attrition rates was noted between treatments. Nabilone was well tolerated, with dizziness/drowsiness most frequently reported.
Conclusion: Nabilone as an adjunctive to GBP is an effective, well-tolerated combination for MS-induced NPP. The results of this study identify a novel therapeutic combination for use in this population of patients predisposed to tolerability issues that may otherwise prevent effective pain management.
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