Parkinson
Studienlage · Detail RCT explorativ (doppelblind, 3 Gruppen) · Parkinson · 2014

Effects of cannabidiol in the treatment of patients with Parkinson’s disease: An exploratory double-blind trial

Gemischt GRADE Moderat 359 Zitate
Stichproben = 21 Pat.
Dauer1 Woche Baseline +…
KontrollePlacebo
EndpunktUPDRS
Verblindungdoppelblind
DesignRCT explorativ (doppelblind, 3 Gruppen)
Cannabinoidcbd
Max. Dosis300.0 mg
Applikationoral
Kernaussage

CBD 300 mg/Tag verbesserte die Lebensqualität (PDQ-39) gegenüber Placebo, ohne Effekt auf Motorik oder Neuroprotektionsmarker.

Zusammenfassung

n=21 Parkinson-Patienten ohne Demenz, CBD 75 mg/d vs. CBD 300 mg/d vs. Placebo (7 pro Gruppe); kein statistisch signifikanter Unterschied in UPDRS-Motorik-Scores; Lebensqualität (PDQ-39 Gesamtscore) signifikant besser in CBD-300-mg-Gruppe vs. Placebo (p=0.05).

P
PopulationParkinson-Patienten ohne Demenz oder psychiatrische Komorbiditäten, n=21
I
InterventionCannabidiol (CBD) 75 mg/Tag oder CBD 300 mg/Tag, oral, 6 Wochen
C
KontrollePlacebo
O
OutcomeKein signifikanter Unterschied bei UPDRS, BDNF oder H1-MRS; PDQ-39 Gesamtscore signifikant besser unter CBD 300 mg/Tag vs. Placebo (p=0,05)
Vertrauen in die Evidenz
Moderat

Dritte von vier GRADE-Stufen, die Effektschätzung ist wahrscheinlich verlässlich.

Herabgestuft wegen
Ungenauigkeit
Qualitätsprofil
Größe
Verblindung Doppelblind
Effektstärke Gemischt
Zitate / Jahr
Autoren
Chagas M H N, Zuardi A W, Tumas V et al.
DOI 10.1177/0269881114550355
Design: RCT explorativ (doppelblind, 3 Gruppen)
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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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