Cannabidiol Pharmacotherapy for Adults With Cannabis Use Disorder

NCT ID: NCT03102918

Last Updated: 2019-01-25

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-02-20
• Study Completion Date: 2017-08-30

Brief Summary

Investigators aim to determine Epidiolex's promise as a pharmacotherapy for cannabis use disorder. Investigators hypothesize that Epidiolex, when added to medical management, will result in greater reductions in marijuana use compared to placebo as measured by the 2 primary outcome measures: 1) quantitative THC levels and 2) self-report by Timeline Follow Back. Secondary outcome measures will include treatment retention, patient satisfaction, cannabis withdrawal, cannabis craving, depressive symptoms, anxiety symptoms, , compliance, and cigarette use.

Detailed Description

Investigators will conduct a Stage 1 pilot feasibility study at McLean Hospital to begin to evaluate Epidiolex as a pharmacotherapy for adults with cannabis use disorder. In this randomized, double-blind, placebo-controlled trial, cannabis-dependent subjects ages 18-65 will receive medical management over a 6-week period, with half receiving Epidiolex treatment and half receiving placebo. Participants will receive either up to 800 mg Epidiolex or placebo over a 6-week treatment period. Following treatment completion, participants will have a follow-up visits at 10 and 14 weeks. Primary outcomes will include self-report of cannabis smoking and results of quantitative urine drug screens for cannabis. Secondary outcome measures will include treatment retention, patient satisfaction, cannabis withdrawal, cannabis craving, depressive symptoms, anxiety symptoms, compliance, and cigarette use.

Conditions

Cannabis Use Disorder

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Cannabidiol

Epidiolex

Group Type: ACTIVE_COMPARATOR

Cannabidiol

Intervention Type: DRUG

Participants will receive either up to 800 mg Epidiolex over a 6-week treatment period.

Placebo

Placebo

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Participants will receive placebo over a 6-week treatment period.

Interventions

Cannabidiol

Participants will receive either up to 800 mg Epidiolex over a 6-week treatment period.

Intervention Type: DRUG

Placebo

Participants will receive placebo over a 6-week treatment period.

Intervention Type: DRUG

Other Intervention Names

Epidiolex

Eligibility Criteria

Inclusion Criteria

• Age range 18-65 years
• DSM 5 diagnosis of cannabis use disorder, based on the Structured Clinical Interview for DSM 5 (SCID-5)
• Express a desire to quit cannabis use within the next 30 days
• Have used cannabis on ≥4 days within the past 30 days (i.e., an average of ≥1 day per week)
• For women of childbearing age, a negative pregnancy test at screening with agreement to use adequate contraception to prevent pregnancy and monthly pregnancy tests; for men, contraception will be discussed at the beginning of the study with the study physician
• Consent for us to communicate with their prescribing clinician
• Furnish the names of 2 locators, who would assist study staff in locating them during the study period
• Live close enough to McLean Hospital to attend study visits
• Plan to stay in the Boston area for the next 3 months
• Are willing and able to sign informed consent

Exclusion Criteria

• Current diagnosis of other drug or alcohol dependence (excluding nicotine)
• Recent (within 3 months) significant cardiac disease
• Current serious psychiatric illness or history of psychosis, schizophrenia, bipolar type I disorder
• Current medical condition (including significant laboratory abnormalities, such as abnormal liver function tests) that could prevent regular study attendance
• Mental retardation or organic mental disorder
• Acutely dangerous or suicidal behavior
• Currently in a residential treatment setting in which substance use is monitored and restricted, since the restricted access to drugs could represent an important confounding variable
• Pregnant, nursing, or, if a woman of childbearing potential, not using a form of birth control judged by the investigator to be effective
• Concomitant daily treatment with opioid analgesics, sedative hypnotics, or other known CNS depressants
• Known hypersensitivity to cannabinoids or sesame oil
• Disease of the gastrointestinal system, liver, or kidneys that may impede metabolism or excretion of CBD
• Inability to read or write in English
• History of seizures, head trauma or other history of CNS insult that could predispose the subject to seizures
• Currently taking valproic acid, lamotrigine, or propranolol, medication metabolized by UGT1A9 or UGT2B7 enzymes (CBD may affect these UGT levels)

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Mclean Hospital

OTHER

Sponsor Role: lead

Responsible Party

Kevin P. Hill, MD, MHS

Assistant Professor of Psychiatry

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

McLean Hospital

Belmont, Massachusetts, United States

Countries

United States

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

2015P002013

Identifier Type: -

Identifier Source: org_study_id