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Trial · NCT05387148

The Efficacy and Neurobehavioural Mechanism of Cannabidiol (CBD) for Alcohol Dependence

NCT05387148, Phase 2, Unknown, South West Sydney Local Health District

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. The Efficacy and Neurobehavioural Mechanism of Cannabidiol (CBD) for Alcohol Dependence. Trials, record NCT05387148. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05387148

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
The Efficacy and Neurobehavioural Mechanism of Cannabidiol (CBD) for Alcohol Dependence
NCT number
NCT05387148
Status
Unknown
Phases
Phase 2
Enrollment
20 participants, estimated
Lead sponsor
South West Sydney Local Health District
Conditions
Alcohol Use Disorder (AUD)
Interventions
Cannabidiol (CBD), Placebo
First posted
2022-05-24
Last updated
2022-06-03

Source ClinicalTrials.gov

Registered outcomes36

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChanges in High Frequency Heart Rate Variability22 daysTo assess whether acute ingestion of CBD can modulate heart rate variability when responding to alcohol cues compared to neutral cues
PrimaryChanges in Skin Conductance Levels22 daysTo assess whether acute ingestion of CBD modulates skin conductance levels when responding to alcohol cues compared to neutral cues
PrimaryChanges in Brain Activation22 daysTo assess whether acute ingestion of CBD can attenuate brain activation via blood oxygen level dependent (BOLD) in areas associated with alcohol cue-elicited craving measured by an fMRI machine
PrimaryChanges in Neurotransmitter levels in the Brain22 daysTo assess whether CBD treatment leads to changes in brain levels of the neurotransmitters: glutamate, gamma-aminobutyric acid (GABA), N-acetylaspartate (NAA) and glutathione (GSH)
PrimaryHeavy Drinking DaysUp to 43 daysReduction in Heavy Drinking Days (HDD; defined as 4 or more drinks in a day for women and five or more drinks in a day for men). This will be measured by the Timeline Follow Back.
PrimaryAbsence of any Heavy Drinking DayUp to 43 daysMeasured by Timeline Follow Back
PrimaryMean Alcohol Consumption per Drinking DayUp to 43 daysMeasured by Timeline Follow Back
PrimaryAlcohol Dependence SeverityBaselineMeasured by the Alcohol Dependence Scale. The minimum score is 0 and the maximum score is 47. A higher score indicates more severe dependence.
PrimaryAlcohol CravingUp to 43 days
As measured by the Penn Alcohol Craving Scale (PACS), which measures the amount of time spent thinking and craving for alcohol, difficulty in resisting consumption of alcohol if present and hypothetical pleasure associated with consumption of alcohol. This scale has a minimum score of 0 and a maximum score of 6. A higher score indicates greater levels of craving.
SecondaryChanges in Alcohol Craving22 days
To assess whether acute ingestion of CBD can modulate subjective measures of alcohol cue elicited craving. This will be measured during the fMRI scan using the Visual Analogue Scale. This scale will assess alcohol craving, thirst and anxiety.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
39252861DERIVED

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests8

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource
1-Back TaskSecondary outcomeConductCognition
2-Back TaskSecondary outcomeConductCognition
Approach-Avoidance TaskSecondary outcomeConductCognition
Balloon RiskSecondary outcomeConductCognition
Columbia Card TaskSecondary outcomeConductCognition
Stroop Color-Word TestSecondary outcomeConductCognition
Trail Making Test ASecondary outcomeConductCognition
Trail Making Test BSecondary outcomeConductCognition

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT05387148

GET https://conductscience.org/api/trials/v1/NCT05387148/registered?page=2