Can ketamine and brain scans help curb alcohol cravings?
NCT ID NCT06969937
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a single dose of ketamine, combined with real-time brain training (neurofeedback), can help people with alcohol use disorder drink less. 75 participants will receive either ketamine or placebo, plus real or fake neurofeedback. The goal is to see if the combination reduces heavy drinking days and changes brain chemistry related to cravings.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Ketamine
- What this could lead to
- If successful, this could point toward a new treatment that helps people with alcohol use disorder reduce their drinking by targeting brain chemistry and cravings.
- What could go wrong
- This is a small, early Phase 2 trial with only 75 participants, so results may not apply to everyone. Ketamine can cause side effects like dissociation or nausea, and the neurofeedback training requires multiple MRI sessions.
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
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 75 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2025
- Expected to finish
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Dec 2026
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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18 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: * Informed Consent as documented by signature * In- and outpatients aged 18 to 65 years of all sexes. * DSM-IV diagnosis of alcohol use disorder (mild - severe). * Motivation to reduce or stop alcohol use * Normal level of language comprehension (German or Swiss-German) * Good physical health with no unstable medical conditions * Participants of childbearing potential must use an effective and established method of contraception for the entire study duration * Comply with the study protocol as explained by investigator Exclusion Criteria: * History of DSM-IV severe drug dependence other than alcohol (except for caffeine or nicotine) and any opiod use disorder within two months prior to enrolment. * Hallucinogen and ketamine use 3 months prior to study participation (including regular microdosing). * Alcohol withdrawal symptoms at any of the treatment visits (V2 and V3) (CIWA-Ar Scale \>9). * Current or lifetime psychotic disorders * History of severe substance-induced psychosis * Current or lifetime bipolar I or II disorders * Current suicidality * Previous suicide attempts during the last 2 years * High risk of adverse emotional and behavioral reactions * Unmedicated or unstable hypertension * Severe illness (e. g. myocardial ischemia or arrythmias, severe pulmonary secretions, glaucoma, congestive heart failure or angina, significant renal or hepatic impairment) * Acute infection (e. g. pulmonary or upper respiratory tract infection) * Insufficient treated or uncorrected hyperthyroidism * Severe central nervous system related traumas or disorders (e. g. stroke, cerebral trauma with loss of consciousness over more than 24h, epilepsy) * During the study, new use or dose changes of already existing concomitant medication without prior informing the investigators. * Taking medications that are known to modualte uridine diphosphate glucuronosyltransferase-enzyme * Medication directly affecting glutamate signaling (e. g. anticonvulsant medication) * Inhibitors of UGT1A9 and 1A10 should be discontinued at least five half-lives prior to the administration of ketamine. * Monoamine oxidase and aldehyde or alcohol dehydrogenase inhibitors should be discontinued at least 5 half-lives prior to the dose of ketamine. * Pregnancy or lactation * Women of childbearing potential with no use of medically accepted contraceptive (e. g. condoms, contraceptive diaphragm, birth control pill, hormone injection, intrauterine device) * BMI \< 17 or \> 35 * Allergy, hypersensitivity, or other adverse reaction to previous use of ketamine * Contradictions to magnetic resonance imaging * Concurrent participation in other clinical study
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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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Psychiatric University Zurich, University of Zurich
RECRUITINGZurich, 8032, Switzerland
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Other studies related to the condition(s) this trial covers.
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- Can a psychedelic compound help veterans and first responders with PTSD and alcohol use disorder?