Does cannabidiol reduce the adverse effects of cannabis in schizophrenia? A randomised, double-blind, cross-over trial




Chesney, Edward; Oliver, Dominic; Sarma, Ananya; Lamper, Ayse Doga; Slimani, Ikram; Lloyd, Millie; Dickens, Alex M.; Welds, Michael; Kråkström, Matilda; Gasparini-Andre, Irma; Oresic, Matej; Lawn, Will; Babayeva, Natavan; Freeman, Tom P.; Englund, Amir; Strang, John; McGuire, Philip

PublisherSpringer Nature

LONDON

2025

Neuropsychopharmacology

Neuropsychopharmacology

NEUROPSYCHOPHARMACOL

9

0893-133X

1740-634X

DOIhttps://doi.org/10.1038/s41386-025-02175-3

https://doi.org/10.1038/s41386-025-02175-3

https://research.utu.fi/converis/portal/detail/Publication/499248716



In patients with schizophrenia, cannabis use exacerbates symptoms and can lead to a relapse of psychosis. Some experimental studies in healthy volunteers suggest that pre-treatment with cannabidiol (CBD) may reduce these effects, but others do not. Here, we investigated whether pre-treatment with CBD ameliorates the acute adverse effects of cannabis in patients with schizophrenia. Participants (n = 30) had schizophrenia or schizoaffective disorder plus a comorbid cannabis use disorder. In a double-blind, randomised, placebo-controlled, crossover trial, participants received oral CBD 1000 mg or placebo three hours before inhaling vaporised cannabis (containing Δ9-tetrahydrocannabinol (THC) 20-60 mg). The primary outcome was delayed verbal recall measured with the Hopkins Verbal Learning Test-Revised. We also measured psychotic symptoms with the Positive and Negative Syndrome Scale (PANSS) - positive subscale. Delayed verbal recall after cannabis administration was 3.5 words (95% confidence interval [CI]: 2.5-4.5) following pre-treatment with CBD, compared to 4.8 words (95% CI: 3.9 to 5.8) following pre-treatment with placebo (mean difference [MD] = -1.3 [95% CI: -2.0 to -0.6]; p = 0.001). After CBD pre-treatment, inhalation of cannabis was associated with an increase in PANSS-P score of 5.0 (95% CI: 3.6 to 6.5), compared to 2.9 (95% CI: 1.5 to 4.3) following pre-treatment with placebo (MD = 2.2 [95% CI: 0.6 to 3.7]; p = 0.01). Administration of CBD did not have a significant effect on plasma concentration of THC or its active metabolite, 11-hydroxy-THC. In patients with schizophrenia and a comorbid cannabis use disorder, pre-treatment with CBD did not attenuate the acute effects of cannabis on memory impairment or psychotic symptoms, but appeared to exacerbate them. The study was registered on Clinicaltrials.gov (NCT04605393).


We would like to thank the staff at the King's Clinical Research Facility and Dr Luke Jelen for their support during the study. We sincerely thank BSPG Laboratories, IPS Pharma, and the Maudsley Hospital Pharmacy for providing and dispensing the study drugs. Without the collaboration of clinicians at the South London and Maudsley NHS Foundation Trust, recruitment for the study would not have been feasible. Finally, we would like to extend our heartfelt appreciation to our participants who generously volunteered their time and efforts to the study.


Last updated on 2025-27-08 at 10:36