Study register · detail
Clear benefit
GRADE
Moderate
101 citations
Samplen = 26 Pat.
Duration8 weeks per treatment phase, 1…
ControlIbuprofen 400 mg/day orally, 8 weeks
EndpointPain intensity
Blindingdoppelblind
DesignRCT (doppelblind, aktiv-kontrolliert, Crossover)
Cannabinoidthc
Max. dose0.5 mg
Routeoral
Key finding
Nabilone reduced pain intensity, analgesic consumption and medication dependence significantly more than ibuprofen.
Summary
n=26 patients with chronic intractable medication overuse headache (MOH), nabilone 0,5 mg/day vs. ibuprofen 400 mg/day, 8-week crossover; nabilone significantly superior for pain intensity (p<0,05) and daily analgesic consumption (p<0,05). Only nabilone reduced degree of medication dependence (−41%, p<0,01) and improved quality of life (p<0,05). First RCT on cannabinoids in MOH.
P
PopulationAdults with treatment-refractory medication overuse headache (MOH), n=30 (26 completers)
I
InterventionNabilone 0,5 mg/day orally, 8 weeks
C
ControlIbuprofen 400 mg/day orally, 8 weeks
O
OutcomeNabilone significantly more effective than ibuprofen for pain intensity and daily analgesic intake (p<0,05); reduction in medication dependence –41% (p<0,01); improvement in quality of life (p<0,05)
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
Medication overuse headache (MOH) is a severe burden to sufferers and its treatment has few evidence-based indications. The aim of this study is to evaluate efficacy and safety of nabilone in reducing pain and frequency of headache, the number of analgesic intake and in increasing the quality of life on patients with long-standing intractable MOH. Thirty MOH patients were enrolled at the University of Modena's Interdepartmental Centre for Research on Headache and Drug Abuse (Italy) in a randomized, double-blind, active-controlled, crossover study comparing nabilone 0.5 mg/day and ibuprofen 400 mg. The patients received each treatment orally for 8 weeks (before nabilone and then ibuprofen or vice versa), with 1 week wash-out between them. Randomization and allocation (ratio 1:1) were carried out by an independent pharmacy through a central computer system. Participants, care givers, and those assessing the outcomes were blinded to treatment sequence. Twenty-six subjects completed the study. Improvements from baseline were observed with both treatments. However, nabilone was more effective than ibuprofen in reducing pain intensity and daily analgesic intake (p < 0.05); moreover, nabilone was the only drug able to reduce the level of medication dependence (-41 %, p < 0.01) and to improve the quality of life (p < 0.05). Side effects were uncommon, mild and disappeared when nabilone was discontinued. This is the first randomized controlled trial demonstrating the benefits of nabilone on headache, analgesic consumption and the quality of life in patients with intractable MOH. This drug also appears to be safe and well-tolerated. Larger scale studies are needed to confirm these preliminary findings.
The impediment to action advances action.