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Cannabidiol: a Novel Intervention for Cannabis Use Problems?

A Phase IIa/b, Randomised, Double-blind, Placebo-controlled, Single-site, Parallel Group Clinical Trial to Examine Cannabidiol (CBD) as a Pharmacological Treatment for Cannabis Dependence.

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02044809
Enrollment
82
Registered
2014-01-24
Start date
2014-03-31
Completion date
2017-06-05
Last updated
2018-10-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cannabis Use Disorder

Brief summary

The purpose of this trial is to investigate a novel treatment for cannabis dependence: cannabidiol. Between 96 and 168 young people who want to quit cannabis and meet criteria for moderate cannabis use disorder (DSM-5) will be recruited from the community. Stage one aims to identify the Most Effective Dose (MEDmg) of oral cannabidiol for reducing cannabis use over four treatment weeks. Stage two will determine whether the MED identified in stage 1 can offer an effective treatment for cannabis dependence.

Interventions

DRUGCannabidiol
DRUGPlacebo

Sponsors

University College, London
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
16 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Aged between 16 and 60 years old. * Meet DSM-5 criteria for moderate cannabis use disorder (≥4 DSM-5 criteria) * Express desire to quit using cannabis within the next four weeks, * Have ≥1 previous failed quit attempt. * Smoke tobacco with cannabis, * Test positive for recent cannabis use according to urine analysis, * Vital signs within healthy limits and have capacity to give consent

Exclusion criteria

* Not willing to use effective contraception from when consent is taken to 6 weeks after treatment has stopped * Positive pregnancy test or breastfeeding * Allergies to the Investigational Medicinal Product (IMP) or placebo and its excipients * \>twice/month use of other illicit drugs * Outside normal Body Mass Index (BMI) * A physical health problem deemed clinically significant * The use of current prescribed psychotropic drugs * Current or prior self-reported diagnosis of a psychotic disorder * Non-English speakers due to verbal assessments.

Design outcomes

Primary

MeasureTime frameDescription
Urinary 11-nor-9-Carboxy-delta-9-tetrahydrocannabinol:creatinine (THC-COOH:creatinine)up to 4 weeksThis study has two stages. This is the primary endpoint criteria for stage 1.
Number of days abstinent from cannabisup to 4 weeksThis study has two stages. This is the primary endpoint criteria for stage 1.
Diagnostic and Statistical Manual- 5 (DSM-5) criteria for moderate cannabis dependenceup to 4 weeksThis study has two stages. This is the primary endpoint criteria for stage 2.
Urinary 11-nor-9-Carboxy-delta-9-tetrahydrocannabinol:creatinine(THC-COOH:creatinine) below 50ng/mlweek 4This study has two stages. This is the primary endpoint criteria for stage 2.

Secondary

MeasureTime frameDescription
Psychological Wellbeing, Cognition and EndocannabinoidsUp to 28 weeksPsychological Wellbeing, Cognition and Endocannabinoids will be measured by questionnaire methods, neuropsychological testing and biological samples.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026