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Anticonvulsant

Lamotrigine for Alcohol Use Disorder

Phase 2
Recruiting
Led By Robert Miranda, PhD
Research Sponsored by Brown University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Self-reports consuming alcohol ≥ 2 days/week on average in the past 90 days of which ≥ 5 days involved ≥ 4 drinks within a 2-hr period (i.e., binge drinking) for boys and ≥ 3 drinks for girls
Females taking estrogen-containing oral contraceptives have to agree to use secondary methods of birth control, such as condoms because lamotrigine lowers the effectiveness of estrogen-containing oral contraceptives. Sexually active females cannot be in this study if they do not agree to use a barrier method of birth control (condom) every time they engage in sexual intercourse.
Must not have
A history of Steven-Johnson syndrome or any presentation of symptoms suggestive of Steven-Johnson syndrome.
Current or lifetime history of psychosis or suicidality
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 9-week active treatment phase
Awards & highlights

Summary

This trial is testing lamotrigine, a medication that stabilizes mood, in teenagers who have problems with alcohol. The goal is to see if it can help reduce their drinking and cravings. Lamotrigine works by balancing brain chemicals that affect mood and behavior. It is known for its efficacy in treating bipolar disorder, particularly in managing depressive symptoms.

Who is the study for?
This trial is for young people aged 16-19 with alcohol use disorder who want to cut down on drinking. They must meet specific criteria for binge drinking and agree to use condoms if they're sexually active females on oral contraceptives. It's not open to those already in AUD treatment, with certain medical conditions or taking conflicting medications.
What is being tested?
The study tests the mood-stabilizer Lamotrigine against a placebo to see if it can help youth reduce their alcohol consumption. Participants will be randomly assigned to either receive Lamotrigine or a placebo, allowing researchers to compare outcomes between the two groups.
What are the potential side effects?
Lamotrigine may cause side effects like skin rashes (potentially serious), dizziness, headaches, blurred vision, nausea, and tiredness. There's also a risk of more severe reactions such as Steven-Johnson syndrome but these are rare.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I have been binge drinking at least 5 days in the last 3 months.
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I agree to use condoms as birth control because I'm on estrogen-based oral contraceptives.
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I am between 16 and 19 years old.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I have had Steven-Johnson syndrome or symptoms like it.
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I have a history of psychosis or suicidal thoughts or actions.
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My kidney tests (BUN and creatinine) show they are not working well.
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I am currently on medication for alcohol use disorder, or taking a carbonic anhydrase inhibitor or a drug that affects glucuronidation.
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I am not taking medications like Depakote, carbamazepine, or rifampin.
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I have kidney or liver problems.
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I have been treated with lamotrigine before.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~9-week active treatment phase
This trial's timeline: 3 weeks for screening, Varies for treatment, and 9-week active treatment phase for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Acceptability of the study medication
Completion rates
Secondary study objectives
Alcohol craving

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: LamotrigineExperimental Treatment1 Intervention
Lamotrigine (25 mg/day to 200 mg/day in two divided doses) for 9 weeks
Group II: PlaceboPlacebo Group1 Intervention
Identical matching placebo capsules
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Lamotrigine
2011
Completed Phase 4
~2490

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for alcoholism work by modulating neurotransmitter activity to restore balance disrupted by chronic alcohol use. Lamotrigine, a mood-stabilizing anticonvulsant, inhibits voltage-sensitive sodium channels, reducing the release of excitatory neurotransmitters like glutamate. Similarly, naltrexone blocks opioid receptors to diminish alcohol's rewarding effects, while acamprosate modulates glutamatergic neurotransmission to ease withdrawal symptoms. These mechanisms are vital for tailoring treatments to address specific neurochemical imbalances in alcoholism patients, improving their chances of recovery.

Find a Location

Who is running the clinical trial?

Brown UniversityLead Sponsor
463 Previous Clinical Trials
618,643 Total Patients Enrolled
29 Trials studying Alcoholism
5,414 Patients Enrolled for Alcoholism
National Institute on Alcohol Abuse and Alcoholism (NIAAA)NIH
823 Previous Clinical Trials
1,161,256 Total Patients Enrolled
432 Trials studying Alcoholism
778,417 Patients Enrolled for Alcoholism
Rhode Island HospitalOTHER
262 Previous Clinical Trials
68,889 Total Patients Enrolled
5 Trials studying Alcoholism
750 Patients Enrolled for Alcoholism

Media Library

Lamotrigine (Anticonvulsant) Clinical Trial Eligibility Overview. Trial Name: NCT04770493 — Phase 2
Alcoholism Research Study Groups: Lamotrigine, Placebo
Alcoholism Clinical Trial 2023: Lamotrigine Highlights & Side Effects. Trial Name: NCT04770493 — Phase 2
Lamotrigine (Anticonvulsant) 2023 Treatment Timeline for Medical Study. Trial Name: NCT04770493 — Phase 2
~14 spots leftby Sep 2025