Study register · detail
No benefit demonstrated
GRADE
Moderate
214 citations
Samplen = 19 Pat.
Duration8 weeks of treatment and 2…
ControlPlacebo oral, 2x daily over 8 weeks
EndpointCDAI
Blindingdoppelblind
DesignRCT
Cannabinoidcbd
Max. dose20.0 mg
Routeoral
Key finding
CBD showed no significant benefit: CDAI decreased in the CBD group from 337±108 to 220±122 and in the placebo group from 308±96 to 216±121 (p=NS); both groups improved similarly.
Summary
n=19 active Crohn's disease, CBD 10 mg 2x daily vs. placebo over 8 weeks; no significant difference in the Crohn's Disease Activity Index (CDAI: -18 vs. -30 points, p=0.6), CBD well tolerated but ineffective at this dose.
P
PopulationAdults with moderately active Crohn's disease (CDAI >200), n=20 (19 completers), refractory to steroids, thiopurines or TNF antagonists
I
InterventionCannabidiol (CBD) 10 mg oral, 2x daily over 8 weeks
C
ControlPlacebo oral, 2x daily over 8 weeks
O
OutcomePrimary endpoint CDAI: baseline CBD 337±108 vs. placebo 308±96, after 8 weeks CBD 220±122 vs. placebo 216±121 (p=n.s.) — no significant difference, CBD safe but not effective
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: Cannabidiol (CBD) is an anti-inflammatory cannabinoid shown to be beneficial in a mouse model of IBD. Lacking any central effect, cannabidiol is an attractive option for treating inflammatory diseases.
Aim: To assess the effects of cannabidiol on Crohn's disease in a randomized placebo-controlled trial.
Patients And Methods: Twenty patients aged 18-75 years with a Crohn's disease activity index (CDAI) >200 were randomized to receive oral (10 mg) CBD or placebo twice daily. Patients did not respond to standard treatment with steroids (11 patients), thiopurines (14), or TNF antagonists (11). Disease activity and laboratory parameters were assessed during 8 weeks of treatment and 2 weeks thereafter. Other medical treatment remained unchanged.
Results: Of 20 patients recruited 19 completed the study. Their mean age was 39 ± 15, and 11 were males. The average CDAI before cannabidiol consumption was 337 ± 108 and 308 ± 96 (p = NS) in the CBD and placebo groups, respectively. After 8 weeks of treatment, the index was 220 ± 122 and 216 ± 121 in the CBD and placebo groups, respectively (p = NS). Hemoglobin, albumin, and kidney and liver function tests remained unchanged. No side effects were observed.
Conclusion: In this study of moderately active Crohn's disease, CBD was safe but had no beneficial effects. This could be due to lack of effect of CBD on Crohn's disease, but could also be due to the small dose of CBD, the small number of patients in the study, or the lack of the necessary synergism with other cannabinoids. Further investigation is warranted.
Clinicaltrials.Gov: NCT01037322.
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