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Cannabidiol as a Treatment for AUD Comorbid With PTSD

Primary Purpose

Alcohol Use Disorder, Post Traumatic Stress Disorder

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Cannabidiol
Placebos
Sponsored by
NYU Langone Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alcohol Use Disorder focused on measuring Cannabidiol

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Males and females age 18-70
  2. DSM-5 diagnosis of moderate or severe AUD
  3. DSM-5 diagnosis of PTSD with Clinician Administered PTSD Scale (CAPS-5) OR subPTSD diagnosis (meeting criterion A, F, G, H and at least 6 symptoms across any criteria B-E) with Clinician Administered PTSD Scale (CAPS-5)
  4. Able to provide voluntary informed consent
  5. At least 6 heavy drinking days (4 or more drinks per day for a woman, 5 or more drinks per day for a man) in the 30 days prior to screen
  6. If of childbearing potential (male or female), are willing to use approved form of contraception from screening for duration of the trial
  7. Able to provide at least two locators
  8. Endorse desire to cut down or stop drinking
  9. Agrees to abstain from all other cannabinoid use for the duration of the study
  10. Confirms they are reliably domiciled

Exclusion Criteria:

  1. Current alcohol withdrawal (CIWA-Ar score >7)
  2. Exclusionary medical conditions (e.g. current severe alcohol withdrawal requiring medical hospitalization, significantly impaired liver function)
  3. DSM-5 diagnosis of schizophrenia, schizoaffective disorder, bipolar disorder
  4. High risk of adverse emotional or behavioral reaction, and/or an inability to understand study procedures or the informed consent process, based on investigator's clinical evaluation (e.g., evidence of serious personality disorder, antisocial behavior, serious current stressors, lack of meaningful social support)
  5. Exposure to trauma in the last 30 days, including police duty or military service
  6. Current significant suicidality (assessed using the C-SSRS), any significant suicidal behavior in the past 12 months, or any history of serious suicide attempts requiring hospitalization, or current significant homicidality
  7. History of Severe Traumatic Brain Injury (TBI; as indicated by Loss of Consciousness > 24 hours)
  8. DSM-5 diagnosis of current mild cannabis use disorder and/or moderate or severe substance use disorder for a substance other than alcohol or nicotine
  9. Significant laboratory abnormalities, including significantly impaired liver function, serious abnormalities of complete blood count or metabolic panel
  10. Active legal problems likely to result in incarceration within 12 weeks of treatment initiation
  11. Pregnancy or lactation
  12. Current use of exclusionary medications, including but not limited to cannabinoids; those acting on serotonergic pathways; treatments for addictions including alcohol; moderate to strong inhibitors of CYP3A4 or CYP2C19; medications metabolized primarily by CYP3A4, CYP3A5, or CYP3A7; and medications with a narrow therapeutic index which are substrates of UGT1A9, UGT2B7, CYP2C8, CYP2C9, CYP2C19, CYP1A2, or CYP2B6.
  13. Current treatment for AUD (with exceptions of: AA/12-step treatment and/or psychosocial treatment initiated more than 3 months prior to the screening visit)
  14. Psychotherapy for PTSD or other psychiatric condition, if initiated within 3 months of screening
  15. Inpatient psychiatric treatment in the last 12 months, with the exception of detox and extended Emergency Department stays
  16. A positive urine drug screen for opioids at screen, baseline, or any later visits. If a participant has a positive drug screen for THC or cocaine at screen, baseline or a later visit- their enrollment will be subject to the clinical judgement of the Principal Investigator.

Sites / Locations

  • New York University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Cannabidiol (CBD 600 mg daily)

Placebo

Arm Description

6 weeks, such that both participants and study staff are blind to treatment condition.

6 weeks, such that both participants and study staff are blind to treatment condition.

Outcomes

Primary Outcome Measures

Number of Drinks Per Day
Number of drinks per day will be assessed by the Time Line Follow Back (TLFB) methodology. TLFB is a drinking assessment method that can be administered in various formats: as clinician-administered interview, paper and pencil and computer. TLFB is used to obtain estimates of the quantity of daily drinking.
Number of Drinks Per Day
Number of drinks per day will be assessed by the Time Line Follow Back (TLFB) methodology. TLFB is a drinking assessment method that can be administered in various formats: as clinician-administered interview, paper and pencil and computer. TLFB is used to obtain estimates of the quantity of daily drinking.
Number of Drinks Per Day
Number of drinks per day will be assessed by the Time Line Follow Back (TLFB) methodology. TLFB is a drinking assessment method that can be administered in various formats: as clinician-administered interview, paper and pencil and computer. TLFB is used to obtain estimates of the quantity of daily drinking.
PCL-5 Total Score
The PCL-5 is a 20-item self-report measure that assesses the 20 Diagnostic and Statistical Manual of Mental Disorders (DSM-5) symptoms of post-traumatic stress disorder (PTSD). The self-report rating scale is 0-4 for each symptom. Rating scale descriptors are the same: "Not at all," "A little bit," Moderately," "Quite a bit," and "Extremely." A total symptom severity score (range - 0-80) can be obtained by summing the scores for each of the 20 items; the higher the score, the more severe the PTSD symptoms.
PCL-5 Total Score
The PCL-5 is a 20-item self-report measure that assesses the 20 Diagnostic and Statistical Manual of Mental Disorders (DSM-5) symptoms of post-traumatic stress disorder (PTSD). The self-report rating scale is 0-4 for each symptom. Rating scale descriptors are the same: "Not at all," "A little bit," Moderately," "Quite a bit," and "Extremely." A total symptom severity score (range - 0-80) can be obtained by summing the scores for each of the 20 items; the higher the score, the more severe the PTSD symptoms.
PCL-5 Total Score
The PCL-5 is a 20-item self-report measure that assesses the 20 Diagnostic and Statistical Manual of Mental Disorders (DSM-5) symptoms of post-traumatic stress disorder (PTSD). The self-report rating scale is 0-4 for each symptom. Rating scale descriptors are the same: "Not at all," "A little bit," Moderately," "Quite a bit," and "Extremely." A total symptom severity score (range - 0-80) can be obtained by summing the scores for each of the 20 items; the higher the score, the more severe the PTSD symptoms.

Secondary Outcome Measures

Percent Carbohydrate Deficient Transferrin (CDT)
CDT test performed on blood sample
Percent Carbohydrate Deficient Transferrin (CDT)
CDT test performed on blood sample
Percent Carbohydrate Deficient Transferrin (CDT)
CDT test performed on blood sample
Percentage of Heavy Drinking Days
Heavy drinking days is defined as 4+ drinks for women or five or more drinks for men per drinking day. This will be averaged for each treatment week.
Percentage of Heavy Drinking Days
Heavy drinking days is defined as 4+ drinks for women or five or more drinks for men per drinking day. This will be averaged for each treatment week.
Percentage of Heavy Drinking Days
Heavy drinking days is defined as 4+ drinks for women or five or more drinks for men per drinking day. This will be averaged for each treatment week.
Percentage of Heavy Drinking Days
Heavy drinking days is defined as 4+ drinks for women or five or more drinks for men per drinking day. This will be averaged for each treatment week.
Percentage of Heavy Drinking Days
Heavy drinking days is defined as 4+ drinks for women or five or more drinks for men per drinking day. This will be averaged for each treatment week.
Percentage of Heavy Drinking Days
Heavy drinking days is defined as 4+ drinks for women or five or more drinks for men per drinking day. This will be averaged for each treatment week.
Percentage of Heavy Drinking Days
Heavy drinking days is defined as 4+ drinks for women or five or more drinks for men per drinking day. This will be averaged for each treatment week.
Percentage of Very Heavy Drinking Days
Very heavy drinking days is defined as 8+/10+ drinks per day for women and men respectively. This will be averaged for each treatment week.
Percentage of Very Heavy Drinking Days
Very heavy drinking days is defined as 8+/10+ drinks per day for women and men respectively. This will be averaged for each treatment week.
Percentage of Very Heavy Drinking Days
Very heavy drinking days is defined as 8+/10+ drinks per day for women and men respectively. This will be averaged for each treatment week.
Percentage of Very Heavy Drinking Days
Very heavy drinking days is defined as 8+/10+ drinks per day for women and men respectively. This will be averaged for each treatment week.
Percentage of Very Heavy Drinking Days
Very heavy drinking days is defined as 8+/10+ drinks per day for women and men respectively. This will be averaged for each treatment week.
Percentage of Very Heavy Drinking Days
Very heavy drinking days is defined as 8+/10+ drinks per day for women and men respectively. This will be averaged for each treatment week.
Percentage of Very Heavy Drinking Days
Very heavy drinking days is defined as 8+/10+ drinks per day for women and men respectively. This will be averaged for each treatment week.
Number of Participants With No Heavy Drinking Days
Number of Participants With No Heavy Drinking Days
Number of Participants With No Heavy Drinking Days
Number of Participants With No Heavy Drinking Days
Number of Participants With No Heavy Drinking Days
Number of Participants With No Heavy Drinking Days
Number of Participants With No Heavy Drinking Days
Number of Participants That Are 'Present and Clear'
Present is defined as present to provide breath alcohol levels (BAC). Clear is defined as having a BAC of zero.
Number of Participants That Are 'Present and Clear'
Present is defined as present to provide breath alcohol levels (BAC). Clear is defined as having a BAC of zero.
Number of Participants That Are 'Present and Clear'
Present is defined as present to provide breath alcohol levels (BAC). Clear is defined as having a BAC of zero.
Number of Participants That Are 'Present and Clear'
Present is defined as present to provide breath alcohol levels (BAC). Clear is defined as having a BAC of zero.
Number of Participants That Are 'Present and Clear'
Present is defined as present to provide breath alcohol levels (BAC). Clear is defined as having a BAC of zero.
Number of Participants That Are 'Present and Clear'
Present is defined as present to provide breath alcohol levels (BAC). Clear is defined as having a BAC of zero.
Number of Participants That Are 'Present and Clear'
Present is defined as present to provide breath alcohol levels (BAC). Clear is defined as having a BAC of zero.
Percentage of Days Abstinent
Percentage of Days Abstinent
Percentage of Days Abstinent
Percentage of Days Abstinent
Percentage of Days Abstinent
Percentage of Days Abstinent
Percentage of Days Abstinent

Full Information

First Posted
August 2, 2017
Last Updated
June 6, 2023
Sponsor
NYU Langone Health
Collaborators
National Institutes of Health (NIH), Tilray
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1. Study Identification

Unique Protocol Identification Number
NCT03248167
Brief Title
Cannabidiol as a Treatment for AUD Comorbid With PTSD
Official Title
Cannabidiol as a Treatment for Alcohol Use Disorder Comorbid With Posttraumatic Stress Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
September 16, 2019 (Actual)
Primary Completion Date
April 20, 2022 (Actual)
Study Completion Date
April 20, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NYU Langone Health
Collaborators
National Institutes of Health (NIH), Tilray

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This project aims to determine whether cannabidiol (CBD), a compound derived from the cannabis plant, is effective in treating alcohol use disorder (AUD) in individuals with comorbid posttraumatic stress disorder (PTSD). Investigators will test the hypothesis that oral cannabidiol (CBD) will reduce alcohol drinking in individuals with AUD comorbid with PTSD. To test this hypothesis, 48 otherwise healthy adult participants with moderate or severe AUD and PTSD will be randomized to treatment with either CBD (600 mg daily) or placebo, for a period of 6 weeks, such that both participants and study staff are blind to treatment condition. Participants (each treated for 6 weeks) will be continuously recruited over a study period of 14 months until 48 have completed. Baseline and weekly data will be collected on alcohol usage and PTSD symptoms, and investigators will assess whether CBD treatment leads to a greater improvement in these measures relative to placebo, and whether reduction in alcohol drinking is temporally linked to improvement in PTSD symptoms. Subjects will also participate in a task designed to quantify the psychological and physiological links between negative emotion produced by re-experiencing PTSD trauma, and alcohol craving. The task will be administered following 4 weeks of treatment. Treatment-associated reduction in alcohol craving elicited by trauma-associated negative emotion between CBD and placebo groups will be compared. This study will be the first to test whether CBD is effective in treating alcohol addiction and in treating PTSD in humans, and the first to examine the interaction between these treatment effects. Results will serve as proof of concept and provide guidance for a future larger clinical trial. Because CBD is a safe, readily available drug, such a trial would have an immense potential to prevent death, medical illness, and psychological suffering associated with AUD and PTSD. Further, because the brain circuits via which CBD acts to produce hypothesized effects are relatively well-understood, results may substantially advance understanding of the neurobiological basis of alcohol addiction.
Detailed Description
In this project, investigators aim to test the hypothesis that CBD will reduce alcohol drinking in individuals with AUD comorbid with PTSD. CBD is currently a medical research focus because it shows promise for treating anxiety and other brain disorders, but does not produce a 'high' like other parts of cannabis, has not been shown to be addictive, and is safe, with few or no side effects. AUD, which is one of the most common and most debilitating psychiatric conditions, is often associated with other comorbid psychiatric disorders - in particular, PTSD: depending on the population studied, 30-60% of individuals with AUD also have PTSD, with high comorbidity rates in military veterans. Evidence from animal models and clinical studies suggests that the negative emotion caused by PTSD symptoms intensifies craving for alcohol during alcohol withdrawal, perpetuating the addictive cycle; further, evidence shows that the brain circuits underlying negative emotion and addiction are linked in a forebrain area called the extended amygdala, which provides a neuropharmacological target to simultaneously treat both negative emotion and alcohol addiction in individuals with AUD and PTSD. CBD is known to inhibit brain activity in the extended amygdala, leading to reduced anxiety in both animal models and humans. CBD also reduces addictive alcohol seeking in animal models.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alcohol Use Disorder, Post Traumatic Stress Disorder
Keywords
Cannabidiol

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
95 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cannabidiol (CBD 600 mg daily)
Arm Type
Experimental
Arm Description
6 weeks, such that both participants and study staff are blind to treatment condition.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
6 weeks, such that both participants and study staff are blind to treatment condition.
Intervention Type
Drug
Intervention Name(s)
Cannabidiol
Other Intervention Name(s)
CBD
Intervention Description
600 mg daily
Intervention Type
Drug
Intervention Name(s)
Placebos
Intervention Description
This project aims to determine whether cannabidiol (CBD) is effective in treating alcohol use disorder (AUD) comorbid posttraumatic stress disorder (PTSD). To address this aim, investigators will conduct a clinical trial in which CBD will be administered to 48 individuals with AUD comorbid with PTSD, and assess alcohol intake and PTSD symptoms. The aim is to test the hypothesis that CBD will reduce alcohol drinking in individuals with AUD comorbid with PTSD. To test this hypothesis, 48 otherwise healthy adult participants with moderate or severe AUD and PTSD will be randomized to treatment with either CBD (600 mg daily) or placebo, for a period of 6 weeks, such that both participants and study staff are blind to treatment condition.
Primary Outcome Measure Information:
Title
Number of Drinks Per Day
Description
Number of drinks per day will be assessed by the Time Line Follow Back (TLFB) methodology. TLFB is a drinking assessment method that can be administered in various formats: as clinician-administered interview, paper and pencil and computer. TLFB is used to obtain estimates of the quantity of daily drinking.
Time Frame
Baseline
Title
Number of Drinks Per Day
Description
Number of drinks per day will be assessed by the Time Line Follow Back (TLFB) methodology. TLFB is a drinking assessment method that can be administered in various formats: as clinician-administered interview, paper and pencil and computer. TLFB is used to obtain estimates of the quantity of daily drinking.
Time Frame
Week 4
Title
Number of Drinks Per Day
Description
Number of drinks per day will be assessed by the Time Line Follow Back (TLFB) methodology. TLFB is a drinking assessment method that can be administered in various formats: as clinician-administered interview, paper and pencil and computer. TLFB is used to obtain estimates of the quantity of daily drinking.
Time Frame
Week 6
Title
PCL-5 Total Score
Description
The PCL-5 is a 20-item self-report measure that assesses the 20 Diagnostic and Statistical Manual of Mental Disorders (DSM-5) symptoms of post-traumatic stress disorder (PTSD). The self-report rating scale is 0-4 for each symptom. Rating scale descriptors are the same: "Not at all," "A little bit," Moderately," "Quite a bit," and "Extremely." A total symptom severity score (range - 0-80) can be obtained by summing the scores for each of the 20 items; the higher the score, the more severe the PTSD symptoms.
Time Frame
Baseline
Title
PCL-5 Total Score
Description
The PCL-5 is a 20-item self-report measure that assesses the 20 Diagnostic and Statistical Manual of Mental Disorders (DSM-5) symptoms of post-traumatic stress disorder (PTSD). The self-report rating scale is 0-4 for each symptom. Rating scale descriptors are the same: "Not at all," "A little bit," Moderately," "Quite a bit," and "Extremely." A total symptom severity score (range - 0-80) can be obtained by summing the scores for each of the 20 items; the higher the score, the more severe the PTSD symptoms.
Time Frame
Week 4
Title
PCL-5 Total Score
Description
The PCL-5 is a 20-item self-report measure that assesses the 20 Diagnostic and Statistical Manual of Mental Disorders (DSM-5) symptoms of post-traumatic stress disorder (PTSD). The self-report rating scale is 0-4 for each symptom. Rating scale descriptors are the same: "Not at all," "A little bit," Moderately," "Quite a bit," and "Extremely." A total symptom severity score (range - 0-80) can be obtained by summing the scores for each of the 20 items; the higher the score, the more severe the PTSD symptoms.
Time Frame
Week 6
Secondary Outcome Measure Information:
Title
Percent Carbohydrate Deficient Transferrin (CDT)
Description
CDT test performed on blood sample
Time Frame
Baseline
Title
Percent Carbohydrate Deficient Transferrin (CDT)
Description
CDT test performed on blood sample
Time Frame
Week 4
Title
Percent Carbohydrate Deficient Transferrin (CDT)
Description
CDT test performed on blood sample
Time Frame
Week 6
Title
Percentage of Heavy Drinking Days
Description
Heavy drinking days is defined as 4+ drinks for women or five or more drinks for men per drinking day. This will be averaged for each treatment week.
Time Frame
Baseline
Title
Percentage of Heavy Drinking Days
Description
Heavy drinking days is defined as 4+ drinks for women or five or more drinks for men per drinking day. This will be averaged for each treatment week.
Time Frame
Week 1
Title
Percentage of Heavy Drinking Days
Description
Heavy drinking days is defined as 4+ drinks for women or five or more drinks for men per drinking day. This will be averaged for each treatment week.
Time Frame
Week 2
Title
Percentage of Heavy Drinking Days
Description
Heavy drinking days is defined as 4+ drinks for women or five or more drinks for men per drinking day. This will be averaged for each treatment week.
Time Frame
Week 3
Title
Percentage of Heavy Drinking Days
Description
Heavy drinking days is defined as 4+ drinks for women or five or more drinks for men per drinking day. This will be averaged for each treatment week.
Time Frame
Week 4
Title
Percentage of Heavy Drinking Days
Description
Heavy drinking days is defined as 4+ drinks for women or five or more drinks for men per drinking day. This will be averaged for each treatment week.
Time Frame
Week 5
Title
Percentage of Heavy Drinking Days
Description
Heavy drinking days is defined as 4+ drinks for women or five or more drinks for men per drinking day. This will be averaged for each treatment week.
Time Frame
Week 6
Title
Percentage of Very Heavy Drinking Days
Description
Very heavy drinking days is defined as 8+/10+ drinks per day for women and men respectively. This will be averaged for each treatment week.
Time Frame
Baseline
Title
Percentage of Very Heavy Drinking Days
Description
Very heavy drinking days is defined as 8+/10+ drinks per day for women and men respectively. This will be averaged for each treatment week.
Time Frame
Week 1
Title
Percentage of Very Heavy Drinking Days
Description
Very heavy drinking days is defined as 8+/10+ drinks per day for women and men respectively. This will be averaged for each treatment week.
Time Frame
Week 2
Title
Percentage of Very Heavy Drinking Days
Description
Very heavy drinking days is defined as 8+/10+ drinks per day for women and men respectively. This will be averaged for each treatment week.
Time Frame
Week 3
Title
Percentage of Very Heavy Drinking Days
Description
Very heavy drinking days is defined as 8+/10+ drinks per day for women and men respectively. This will be averaged for each treatment week.
Time Frame
Week 4
Title
Percentage of Very Heavy Drinking Days
Description
Very heavy drinking days is defined as 8+/10+ drinks per day for women and men respectively. This will be averaged for each treatment week.
Time Frame
Week 5
Title
Percentage of Very Heavy Drinking Days
Description
Very heavy drinking days is defined as 8+/10+ drinks per day for women and men respectively. This will be averaged for each treatment week.
Time Frame
Week 6
Title
Number of Participants With No Heavy Drinking Days
Time Frame
Baseline
Title
Number of Participants With No Heavy Drinking Days
Time Frame
Week 1
Title
Number of Participants With No Heavy Drinking Days
Time Frame
Week 2
Title
Number of Participants With No Heavy Drinking Days
Time Frame
Week 3
Title
Number of Participants With No Heavy Drinking Days
Time Frame
Week 4
Title
Number of Participants With No Heavy Drinking Days
Time Frame
Week 5
Title
Number of Participants With No Heavy Drinking Days
Time Frame
Week 6
Title
Number of Participants That Are 'Present and Clear'
Description
Present is defined as present to provide breath alcohol levels (BAC). Clear is defined as having a BAC of zero.
Time Frame
Baseline
Title
Number of Participants That Are 'Present and Clear'
Description
Present is defined as present to provide breath alcohol levels (BAC). Clear is defined as having a BAC of zero.
Time Frame
Week 1
Title
Number of Participants That Are 'Present and Clear'
Description
Present is defined as present to provide breath alcohol levels (BAC). Clear is defined as having a BAC of zero.
Time Frame
Week 2
Title
Number of Participants That Are 'Present and Clear'
Description
Present is defined as present to provide breath alcohol levels (BAC). Clear is defined as having a BAC of zero.
Time Frame
Week 3
Title
Number of Participants That Are 'Present and Clear'
Description
Present is defined as present to provide breath alcohol levels (BAC). Clear is defined as having a BAC of zero.
Time Frame
Week 4
Title
Number of Participants That Are 'Present and Clear'
Description
Present is defined as present to provide breath alcohol levels (BAC). Clear is defined as having a BAC of zero.
Time Frame
Week 5
Title
Number of Participants That Are 'Present and Clear'
Description
Present is defined as present to provide breath alcohol levels (BAC). Clear is defined as having a BAC of zero.
Time Frame
Week 6
Title
Percentage of Days Abstinent
Time Frame
Baseline
Title
Percentage of Days Abstinent
Time Frame
Week 1
Title
Percentage of Days Abstinent
Time Frame
Week 2
Title
Percentage of Days Abstinent
Time Frame
Week 3
Title
Percentage of Days Abstinent
Time Frame
Week 4
Title
Percentage of Days Abstinent
Time Frame
Week 5
Title
Percentage of Days Abstinent
Time Frame
Week 6

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males and females age 18-70 DSM-5 diagnosis of moderate or severe AUD DSM-5 diagnosis of PTSD with Clinician Administered PTSD Scale (CAPS-5) OR subPTSD diagnosis (meeting criterion A, F, G, H and at least 6 symptoms across any criteria B-E) with Clinician Administered PTSD Scale (CAPS-5) Able to provide voluntary informed consent At least 6 heavy drinking days (4 or more drinks per day for a woman, 5 or more drinks per day for a man) in the 30 days prior to screen If of childbearing potential (male or female), are willing to use approved form of contraception from screening for duration of the trial Able to provide at least two locators Endorse desire to cut down or stop drinking Agrees to abstain from all other cannabinoid use for the duration of the study Confirms they are reliably domiciled Exclusion Criteria: Current alcohol withdrawal (CIWA-Ar score >7) Exclusionary medical conditions (e.g. current severe alcohol withdrawal requiring medical hospitalization, significantly impaired liver function) DSM-5 diagnosis of schizophrenia, schizoaffective disorder, bipolar disorder High risk of adverse emotional or behavioral reaction, and/or an inability to understand study procedures or the informed consent process, based on investigator's clinical evaluation (e.g., evidence of serious personality disorder, antisocial behavior, serious current stressors, lack of meaningful social support) Exposure to trauma in the last 30 days, including police duty or military service Current significant suicidality (assessed using the C-SSRS), any significant suicidal behavior in the past 12 months, or any history of serious suicide attempts requiring hospitalization, or current significant homicidality History of Severe Traumatic Brain Injury (TBI; as indicated by Loss of Consciousness > 24 hours) DSM-5 diagnosis of current mild cannabis use disorder and/or moderate or severe substance use disorder for a substance other than alcohol or nicotine Significant laboratory abnormalities, including significantly impaired liver function, serious abnormalities of complete blood count or metabolic panel Active legal problems likely to result in incarceration within 12 weeks of treatment initiation Pregnancy or lactation Current use of exclusionary medications, including but not limited to cannabinoids; those acting on serotonergic pathways; treatments for addictions including alcohol; moderate to strong inhibitors of CYP3A4 or CYP2C19; medications metabolized primarily by CYP3A4, CYP3A5, or CYP3A7; and medications with a narrow therapeutic index which are substrates of UGT1A9, UGT2B7, CYP2C8, CYP2C9, CYP2C19, CYP1A2, or CYP2B6. Current treatment for AUD (with exceptions of: AA/12-step treatment and/or psychosocial treatment initiated more than 3 months prior to the screening visit) Psychotherapy for PTSD or other psychiatric condition, if initiated within 3 months of screening Inpatient psychiatric treatment in the last 12 months, with the exception of detox and extended Emergency Department stays A positive urine drug screen for opioids at screen, baseline, or any later visits. If a participant has a positive drug screen for THC or cocaine at screen, baseline or a later visit- their enrollment will be subject to the clinical judgement of the Principal Investigator.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charles Marmar, MD
Organizational Affiliation
New York University Grossman School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
New York University School of Medicine
City
New York
State/Province
New York
ZIP/Postal Code
10016
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Cannabidiol as a Treatment for AUD Comorbid With PTSD

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