Evidence map›Paper›PMID 40357520›Full record

ArticleFrontiers in psychiatry2025

A preliminary randomized trial of the safety, tolerability, and clinical effects of hemp-derived cannabidiol in alcohol use disorder.

Raeghan L Mueller, Jake F Hooper, Jarrod M Ellingson, Aviva K Olsavsky, Rachael Rzasa-Lynn, Angela D Bryan, L Cinnamon Bidwell, Kent E Hutchison

Abstract read
In one paragraph

Article in Frontiers in psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Raeghan L MuellerDepartment of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Jake F HooperDepartment of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Jarrod M EllingsonDepartment of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Aviva K OlsavskyDepartment of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Rachael Rzasa-LynnDepartment of Anesthesiology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Angela D BryanDepartment of Psychology and Neuroscience, University of Colorado Boulder, Boulder, CO, United States.
L Cinnamon BidwellDepartment of Psychology and Neuroscience, University of Colorado Boulder, Boulder, CO, United States.
Kent E HutchisonDepartment of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.

Funding

AACAP Physician Scientist Program in Substance UseK12DA000357 · NIDA · AMERICAN ACADEMY-CHILD/ADOLESCENT PSYCH · PI Kevin M. Gray · 1998 to 2026
$29.1M
Rocky Mountain Cannabis Research CenterP50DA056408 · NIDA · UNIVERSITY OF COLORADO DENVER · PI Angela Bryan · 2023 to 2026
$14.0M
Alcohol Use Disorder and Cannabis: Testing Novel Harm Reduction StrategiesR01AA029606 · NIAAA · UNIVERSITY OF COLORADO DENVER · PI KENT E. HUTCHISON · 2022 to 2026
$2.5M
NIAAA NIH HHS R01 AA029606NIDA NIH HHS K12 DA000357NIDA NIH HHS P50 DA056408
6 · The paper itself

Abstract

Introduction: Cannabidiol (CBD) has recently gained attention for its potential therapeutic effects in substance use disorders, including Alcohol Use Disorder (AUD). This study examined the potential therapeutic effects of commercially available products containing CBD with and without a small amount of tetrahydrocannabinol (THC) on alcohol use and craving among individuals with moderate to severe AUD. Methods: In this feasibility study, a total of 44 participants were randomized to one of three conditions: full-spectrum CBD ( Results: Analyses of attrition and side effect data indicated no significant differences across conditions, suggesting that both bsCBD and fsCBD were well tolerated. Individuals receiving fsCBD demonstrated reductions in craving but no reduction in drinks per drinking day. Discussion: In this pilot study, safety profiles fsCBD and bsCBD were similar, and fsCBD was associated with a greater reduction in craving and AUD symptoms relative to both bsCBD and placebo. Future studies with larger sample sizes will be necessary to replicate and extend these findings by addressing the question of whether a small amount of THC may work synergistically with CBD.

Indexed as

alcoholismalcohol use disordercannabidiolcannabinoidsclinical trialthc

Identifiers

PMID40357520
PMCPMC12066606

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.