Study register · detail
Mixed
GRADE
Moderate
359 citations
Samplen = 21 Pat.
Duration1 week baseline + treatment…
ControlPlacebo
EndpointUPDRS
Blindingdoppelblind
DesignRCT explorativ (doppelblind, 3 Gruppen)
Cannabinoidcbd
Max. dose300.0 mg
Routeoral
Key finding
CBD 300 mg/day improved quality of life (PDQ-39) versus placebo, with no effect on motor function or neuroprotection markers.
Summary
n=21 Parkinson's patients without dementia, CBD 75 mg/d vs. CBD 300 mg/d vs. placebo (7 per group); no statistically significant difference in UPDRS motor scores; quality of life (PDQ-39 total score) significantly better in the CBD 300 mg group vs. placebo (p=0.05).
P
PopulationParkinson's patients without dementia or psychiatric comorbidities, n=21
I
InterventionCannabidiol (CBD) 75 mg/day or CBD 300 mg/day, oral, 6 weeks
C
ControlPlacebo
O
OutcomeNo significant difference in UPDRS, BDNF or H1-MRS; PDQ-39 total score significantly better under CBD 300 mg/day vs. placebo (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
Mixed
Citations / year
★★★★★
Authors
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Abstract
<h4>Introduction</h4>Parkinson's disease (PD) has a progressive course and is characterized by the degeneration of dopaminergic neurons. Although no neuroprotective treatments for PD have been found to date, the endocannabinoid system has emerged as a promising target.<h4>Methods</h4>From a sample of 119 patients consecutively evaluated in a specialized movement disorders outpatient clinic, we selected 21 PD patients without dementia or comorbid psychiatric conditions. Participants were assigned to three groups of seven subjects each who were treated with placebo, cannabidiol (CBD) 75 mg/day or CBD 300 mg/day. One week before the trial and in the last week of treatment participants were assessed in respect to (i) motor and general symptoms score (UPDRS); (ii) well-being and quality of life (PDQ-39); and (iii) possible neuroprotective effects (BDNF and H(1)-MRS).<h4>Results</h4>We found no statistically significant differences in UPDRS scores, plasma BDNF levels or H(1)-MRS measures. However, the groups treated with placebo and CBD 300 mg/day had significantly different mean total scores in the PDQ-39 (p = 0.05).<h4>Conclusions</h4>Our findings point to a possible effect of CBD in improving quality of life measures in PD patients with no psychiatric comorbidities; however, studies with larger samples and specific objectives are required before definitive conclusions can be drawn.
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