Study register · detail
Clear benefit
GRADE
Moderate
346 citations
Samplen = 7 Pat.
ControlPlacebo
EndpointLevodopa-induced dyskinesia
Blindingdoppelblind
DesignRCT (crossover)
Cannabinoidthc
Routeoral
Key finding
Nabilone significantly reduces levodopa-induced dyskinesia in Parkinson's patients versus placebo.
Summary
n=7 Parkinson's patients with levodopa-induced dyskinesia, nabilone (cannabinoid receptor agonist) vs. placebo (randomised, double-blind, crossover); nabilone significantly reduced levodopa-induced dyskinesia (p<0.05 implied).
P
PopulationParkinson's patients with levodopa-induced dyskinesia, n=7
I
InterventionNabilone (cannabinoid receptor agonist), oral
C
ControlPlacebo
O
OutcomeNabilone significantly reduces levodopa-induced dyskinesia vs. placebo
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
The lateral segment of the globus pallidus (GPl) is thought to be overactive in levodopa-induced dyskinesia in PD. Stimulation of cannabinoid receptors in the GPl reduces gamma-aminobutyric acid (GABA) reuptake and enhances GABA transmission and may thus alleviate dyskinesia. In a randomized, double-blind, placebo-controlled, crossover trial (n = 7), the authors demonstrate that the cannabinoid receptor agonist nabilone significantly reduces levodopa-induced dyskinesia in PD.
The impediment to action advances action.