Study register · detail
No benefit demonstrated
GRADE
Moderate
0 citations
Samplen = 28 Pat.
Durationup to week 8
ControlPlacebo
EndpointPASI
Blindingdoppelblind
DesignRCT
Cannabinoidcbd
Max. dose60.0 mg
Routeoral
Key finding
CBD oil did not lead to a significant improvement in psoriasis severity (PASI scores), but showed temporary improvements in itch and sleep onset latency.
Summary
RCT (n=28) on oral CBD oil 60 mg/day vs. placebo in chronic plaque psoriasis over 8 weeks. Primary endpoint (PASI) not significantly improved. Secondary: significant itch reduction (itch score) up to week 8; sleep onset latency decreased up to week 6 (not sustained). Adverse effects mild to moderate, comparable to placebo. Primarily psoriasis — pruritus as secondary outcome.
P
PopulationAdults with chronic plaque psoriasis, n=28
I
InterventionOral CBD oil 60 mg/day
C
ControlPlacebo
O
OutcomeNo significant difference in PASI score between CBD and placebo; significant reduction in itch score up to week 8 and temporary shortening of sleep onset latency up to week 6 (not sustained)
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
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Abstract
Background: The management of psoriasis presents challenges, prompting many patients to seek alternative treatments. Cannabidiol (CBD) has demonstrated potential antioxidant and anti-inflammatory properties which may offer therapeutic benefits for skin conditions.
Objective: To evaluate the efficacy and safety of cannabidiol oil compared to placebo in chronic plaque psoriasis patients.
Methods: The randomized, double-blind, placebo-controlled trial enrolled 28 participants, who were administered either oral CBD oil 60 mg/day or placebo. The primary outcome was the Psoriasis Area and Severity Index (PASI) score. Secondary outcomes encompassed disease severity, quality of life, and sleep parameters. Safety was monitored through adverse events and laboratory assessments.
Results: The CBD group did not demonstrate a significant improvement in PASI scores. However, there was a notable reduction in itch scores by Week 8, and sleep onset latency decreased by Week 6, although this effect was not sustained. Adverse events were mild to moderate in nature and similar across both groups.
Limitations: The study duration may not fully capture the long-term effects, and the race and disease severity may limit the generalizability of the findings. A larger sample size is suggested for future studies.
Conclusion: Cannabidiol oil was well-tolerated; however, it did not result in a significant reduction in psoriasis severity. Temporary improvements in itch relief and sleep onset indicate that further research with higher doses and extended durations is warranted.
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