Could CBD ease alcohol withdrawal? new trial aims to find out
NCT ID NCT07148843
First seen Jun 27, 2026 · Last updated Aug 19, 2026 · Updated 3 times
Summary
This study tests whether cannabidiol (CBD), a compound from cannabis, can reduce alcohol withdrawal symptoms and cravings in people with moderate-to-severe alcohol use disorder. 105 adults will stay in a hospital for 5 days, receive either CBD or a placebo alongside standard care, and have their withdrawal, sleep, and cravings measured. The goal is to see if CBD offers a safe, non-addictive way to ease the detox process.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Cannabidiol (CBD)
- What this could lead to
- If it works, CBD could become a safe, non-addictive option to help people manage alcohol withdrawal and reduce cravings during detox.
- What could go wrong
- This is an early-stage trial with only 105 participants, so results may not apply to everyone. CBD's effects on withdrawal are still unproven in humans, and it may not outperform standard care.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
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About 105 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2030
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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21 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria * Meets DSM-5 criteria Moderate or Severe Alcohol Use Disorder * Age 21-65 * Report at least one prior episode of alcohol withdrawal symptoms at least one day in duration that caused significant impairment in functioning (i.e., unable to attend work or engage in typical activities) AND/OR required medications to manage symptoms. * Drinking at least 8 drinks a day over the two weeks prior to screening. * Negative human chorionic gonadotropin (hCG) on qualitative urine pregnancy screen * Shipley vocabulary score \> 18, corresponding to 5th grade reading level. * Demonstrated understanding of informed consent and ability to consent to participation in the study. Exclusion Criteria * Current or past alcohol-related medical complications including but not limited to cirrhosis of the liver, esophageal varices, pancreatitis, severe gastritis, hemoptysis, hematochezia, or melena. * Use of gabapentin, benzodiazepines, or other sedative-hypnotic medications within the week prior to admission * Regular use (e.g., more than twice a week) of cannabis or CBD products. * Regular use of benzodiazepines (e.g., twice a week or more) within the last three months * Meet DSM-5 criteria for moderate-to-severe substance use disorder (SUD), including Cannabis Use Disorder (except for alcohol and tobacco) * Urine drug screen indicating the presence of substances other than cannabis at screening. * Unstable and/or compromising medical or psychiatric conditions that would interfere with participant safety as determined by study physician. * Current pregnancy * BMI \<17 * History of anorexia nervosa or bulimia in the past 2 years * History of seizures or seizure disorder outside of alcohol-withdrawal related seizures * Systolic blood pressure (SBP) \> 180, Diastolic Blood Pressure (DBP) \> 120 or pulse \> 120 during screening or upon admission * Any of the following laboratory values during screening or upon admission: * AST \> 165 U/L (normal range 19-55) * ALT \> 216 U/L (normal range 19-72) * Alkaline phosphatase \> 378 U/L (normal range 38-126) * Total bilirubin \>2.5 mg/dl (normal values=0.3-1.0 mg/dL) * Non-fasting glucose \> 250 mg/ml (normal range 65-179) * Hematocrit \< 38 % (normal range 41-53) * Hemoglobin \< 12 g/dl (normal range 13.5-17.5) or any other laboratory value significantly outside the normal range * Use of a prescription medication (except for birth control prescriptions) within 14 days of study entry, which, in the opinion of the investigator or sponsor, will interfere with the study result or the safety of the subject. This includes any medication in which CYP2C9, CYP2C19, CYP1A2, CYP2B10, or CYP3A4 enzymes are major metabolizers. * ECG with corrected QT interval (QTC) \>/= 500 ms and/or presence of clinically significant abnormality * Participation in other clinical trials within the past 60 days * Court-mandated participation in alcohol treatment or pending incarceration
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Behavioral Pharmacology Research Unit
Baltimore, Maryland, 21224, United States
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Other studies related to the condition(s) this trial covers.
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- Can a bike ride curb drinking and heal the liver?
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- Can just seeing and smelling a drink trigger alcohol cravings?
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