Parkinson Disease
Study register · detail RCT · Parkinson Disease · 2024

Short-Term Cannabidiol with Delta-9-Tetrahydrocannabinol in Parkinson's Disease: A Randomized Trial.

No benefit demonstrated GRADE Moderate 19 citations
Samplen = 61 Pat.
Duration2 weeks, then observation until…
ControlPlacebo
EndpointMDS-UPDRS Motor
Blindingdoppelblind
DesignRCT
Cannabinoidkombination
THC:CBD1:30
Routeoral
Key finding

CBD/THC showed no significant benefit over placebo on motor MDS-UPDRS (difference -1,80, p=0,379); placebo was possibly superior for sleep and cognition, with more adverse effects in the CBD/THC group.

Summary

RCT n=61 (CBD/THC n=31, placebo n=30), 2 weeks titration to final dose 191,8±48,9 mg CBD + 6,4±1,6 mg THC daily. Primary endpoint motor MDS-UPDRS: reduction -4,57 (95% CI -8,11 to -1,03; p=0,013) in CBD/THC group vs. -2,77 (-4,92 to -0,61; p=0,014) in placebo; group difference not significant: -1,80 (-5,88 to 2,27; p=0,379). No benefit, possibly worsened cognition and sleep; strong placebo effect. Adverse effects mild, more frequent in CBD/THC group.

P
PopulationPersons with Parkinson's disease (MDS-UPDRS Motor ≥20, cannabis-naive), n=61
I
InterventionOral cannabis extract (CBD/THC in sesame oil), 2,5 mg/kg/day, of which ~191,8 mg CBD + 6,4 mg THC daily, 2 weeks
C
ControlPlacebo (oral sesame oil)
O
OutcomeMotor MDS-UPDRS: reduction of 4,57 points (CBD/THC) vs. 2,77 points (placebo); group difference not significant: −1,80 (95% CI −5,88 to 2,27; p=0,379)
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 No benefit
Citations / year
Authors
Liu Y, Bainbridge J, Sillau S, Rajkovic S, Adkins M, Domen CH, Thompson JA, Seawalt T, Klawitter J, Sempio C
DOI 10.1002/mds.29768
Design: RCT
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Abstract
Background: Cannabis use is frequent in Parkinson's disease (PD), despite inadequate evidence of benefits and risks. Objective: The aim is to study short-term efficacy and tolerability of relatively high cannabidiol (CBD)/low Delta-9-tetrahydrocannabinol (THC) to provide preliminary data for a longer trial. Methods: Persons with PD with >/=20 on motor Movement Disorder Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS) who had negative cannabis testing took cannabis extract (National Institute of Drug Abuse) oral sesame oil solution for 2 weeks, increasing to final dose of 2.5 mg/kg/day. Primary outcome was change in motor MDS-UPDRS from baseline to final dose. Results: Participants were randomized to CBD/THC (n = 31) or placebo (n = 30). Mean final dose (CBD/THC group) was 191.8 +/- 48.9 mg CBD and 6.4 +/- 1.6 mg THC daily. Motor MDS-UPDRS was reduced by 4.57 (95% CI, -8.11 to -1.03; P = 0.013) in CBD/THC group, and 2.77 (-4.92 to -0.61; P = 0.014) in placebo; the difference between groups was non-significant: -1.80 (-5.88 to 2.27; P = 0.379). Several assessments had a strong placebo response. Sleep, cognition, and activities of daily living showed a treatment effect, favoring placebo. Overall adverse events were mild and reported more in CBD/THC than placebo group. On 2.5 mg/kg/day CBD plasma level was 54.0 +/- 33.8 ng/mL; THC 1.06 +/- 0.91 ng/mL. Conclusions: The brief duration and strong placebo response limits interpretation of effects, but there was no benefit, perhaps worsened cognition and sleep, and there was many mild adverse events. Longer duration high quality trials that monitor cannabinoid concentrations are essential and would require improved availability of research cannabinoid products in the United States. (c) 2024 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

The impediment to action advances action. — Marcus Aurelius