Anxiety During Abstinence in AUD
Columbia University · with National Institute on Alcohol Abuse and Alcoholism (NIAAA) · NCT06793488
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 21–55 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Early Phase 1
- Target enrollment
- 60
- US sites recruiting
- 1
- Study start
- September 15, 2025
- Record last updated
- February 10, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The goal of this study is to better understand the underlying neurobiological basis of anxiety that emerges during abstinence in patients with alcohol use disorder (AUD). The main questions it aims to answer are:
- To characterize anxiety itself as well as anxiety related-neurobiological circuitry in early abstinence in AUD
- To examine how anxiety and anxiety related-neurobiological circuitry change over the course of abstinence in AUD
Researchers will recruit both participants with AUD and healthy volunteers.
The participants with AUD will be prescribed disulfiram, a medication that helps participants with AUD stay abstinent. Healthy volunteers will not receive antabuse. Patients with AUD will undergo fMRI scanning both after 1 week and 3 months of disulfiram treatment. Healthy volunteers will undergo fMRI once.
Being studied: Disulfiram 250 mg; functional MRI
Conditions: Alcohol Use Disorder
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria (Participants with Alcohol use Disorder):
- Between the ages of 21 and 55
- Right-handed
- Able to perform informed consent and comply with study
- Seeking treatment for AUD
- Meets The Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria for AUD of at least moderate severity (>3 symptoms)
Inclusion Criteria (Healthy Volunteer Participants):
- Between the ages of 21 and 55
- Right-handed
- Able to perform informed consent and comply with study
- Report drinking an average of fewer than 8/15 standard drinks per week for women/men and no more than 1 HDD (heavy drinking days) during the previous 28 days.
Exclusion Criteria (Participants with Alcohol use Disorder):
- Neurological, medical or other conditions that would interfere with MRI scanning (e.g., history of stroke, seizure, brain tumor, brain infection, traumatic brain injury, multiple sclerosis, dementia, non MRI-compliant metal device in body, pregnancy, claustrophobia, color blindness, severe hearing impairment, weight>300 lbs., wheelchair-bound, tattoos as indicated by the guidelines established by the Zuckerman Institute MRI unit: https://mr.research.columbia.edu/
- DSM 5 diagnoses of schizophrenia, schizoaffective disorder, or bipolar disorder
- Any non-AUD psychiatric disorder that may, according to the investigator's judgment, require treatment over the course of the study
- Significant suicide or violence risk
- Currently taking psychotropic medication
- Current substance use disorder other than AUD, tobacco use disorder or mild cannabis use disorder
- Currently pregnant, attempting to become pregnant or nursing
- Sufficiently socially unstable as to preclude participation (e.g. homeless).
- Known history of allergy, intolerance, or hypersensitivity to disulfiram or its derivates
- Contraindications to disulfiram treatment (e.g. liver disease, kidney disease, cardiac disease, seizure disorder, hypothyroidism, diabetes mellitus, pregnancy or lactation, allergy to disulfiram or thiuram derivatives)
- Currently taking medications containing alcohol, metronidazole, isoniazid, paraldehyde, phenytoin, warfarin, or theophylline.
- Treatment with concomitant medications that might interfere with disulfiram
- A history of alcohol withdrawal seizures, delirium tremens or resistant alcohol withdrawal
- Current moderate or severe alcohol withdrawal (CIWA >9 with BAL\<0.05)
- History of prior disulfiram treatment failure
- Being abstinent for > 7 days at the time of screening
Exclusion Criteria (Healthy Volunteer Participants):
- Neurological, medical or other conditions that would interfere with MRI scanning (e.g., history of stroke, seizure, brain tumor, brain infection, traumatic brain injury, multiple sclerosis, dementia, non MRI-compliant metal device in body, pregnancy, claustrophobia, color blindness, severe hearing impairment, weight>300 lbs., wheelchair- bound, tattoos as indicated by the guidelines established by the ZI MRI unit: https://mr.research.columbia.edu/
- DSM 5 diagnoses of schizophrenia, schizoaffective disorder, or bipolar disorder
- Any psychiatric disorder that may, according to the investigator's judgment, require treatment over the course of the study
- Significant suicide or violence risk
- Currently taking psychotropic medication
- Current substance use disorder other than tobacco use disorder or mild cannabis use disorder
- Currently pregnant, attempting to become pregnant or nursing
- Sufficiently socially unstable as to preclude participation (e.g., homeless).
- A diagnosis of AUD of any severity
Recruiting US locations
Columbia University Irving Medical Center
New York, NY 10019
Site contact: A B Srivastava, MD · 646-774-8189 · abs2257@cumc.columbia.edu
Study contacts (from the official record)
- A B Srivastava, MD · 646-774-8189 · abs2257@cumc.columbia.edu
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