Chronic Pain
Study register · detail RCT (randomisiert, doppelblind, placebokontrolliert) · Chronic Pain · 2022

Cannabidiol treatment in hand osteoarthritis and psoriatic arthritis: a randomized, double-blind, placebo-controlled trial

No benefit demonstrated GRADE High 101 citations
Samplen = 129 Pat.
Duration12 weeks
ControlPlacebo daily orally
EndpointPain intensity
Blindingdoppelblind
DesignRCT (randomisiert, doppelblind, placebokontrolliert)
Cannabinoidcbd
Max. dose30.0 mg
Routeoral
Key finding

CBD 20–30 mg/day did not significantly reduce pain intensity compared with placebo.

Summary

RCT (n=129) on synthetic CBD 20–30 mg/day vs. placebo over 12 weeks in hand osteoarthritis and psoriatic arthritis; group difference in pain intensity after 12 weeks: 0,23 mm (95%-CI −9,41 to 9,90; p=0,96) — no clinically or statistically significant pain effect. 22% CBD vs. 21% placebo group achieved >30 mm pain reduction.

P
PopulationAdults with hand osteoarthritis or psoriatic arthritis and moderate pain intensity despite existing therapy, n=129 (randomised n=136)
I
InterventionSynthetic CBD 20–30 mg/day orally as add-on therapy
C
ControlPlacebo daily orally
O
OutcomeNo significant difference in pain intensity after 12 weeks: group difference 0,23 mm (95% CI −9,41 to 9,90; p=0,96)
Confidence in the evidence
High

The highest of four GRADE levels, the effect estimate is very reliable.

Quality profile
Sample size
Blinding Double-blind
Effect size No benefit
Citations / year
Authors
Vela J, Dreyer L, Petersen K K et al.
DOI 10.1097/j.pain.0000000000002466
Design: RCT (randomisiert, doppelblind, placebokontrolliert)
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Abstract
<h4>Abstract</h4>Cannabidiol (CBD) is increasingly used as analgesic medication although the recent International Association for the Study of Pain Presidential Task Force on cannabis and cannabinoid analgesia found a lack of trials examining CBD for pain management. This trial examines CBD as add-on analgesic therapy in patients with hand osteoarthritis or psoriatic arthritis experiencing moderate pain intensity despite therapy. Using a randomized, double-blind, placebo-controlled design, patients received synthetic CBD 20 to 30 mg or placebo daily for 12 weeks. The primary outcome was pain intensity during the past 24 hours (0-100 mm); safety outcomes were percentage of patients experiencing adverse events and a characterization of serious adverse events. Explorative outcomes included change in Pittsburgh Sleep Quality Index, Hospital Anxiety and Depression Scale, Pain Catastrophizing Scale (PCS), and Health Assessment Questionnaire Disability Index. One hundred thirty-six patients were randomized, of which 129 were included in the primary analysis. Between-group difference in pain intensity at 12 weeks was 0.23 mm (95% confidence interval -9.41 to 9.90; P = 0.96). Twenty-two percent patients receiving CBD and 21% receiving placebo experienced a reduction in pain intensity of more than 30 mm. We found neither clinically nor statistically significant effects of CBD for pain intensity in patients with hand osteoarthritis and psoriatic arthritis when compared with placebo. In addition, no statistically significant effects were found on sleep quality, depression, anxiety, or pain catastrophizing scores.

The impediment to action advances action. — Marcus Aurelius