The Role of Brief Potent Glutamatergic Modulation in Addressing Problem Drinking

Description

The proposed project tests the efficacy of glutamate modulators in non-depressed individuals with alcohol use disorder (AUD); the primary hypothesis is that the glutamate modulator being tested reduces heavy drinking days compared to the active control. It also aims to investigate, using a 2 by 2 factorial (2x2) design, the hypothesis that the effects of the glutamate modulator are enhanced when combined with behavioral treatment.

Conditions

Alcohol Use Disorder

Study Overview

Study Details

Study overview

The proposed project tests the efficacy of glutamate modulators in non-depressed individuals with alcohol use disorder (AUD); the primary hypothesis is that the glutamate modulator being tested reduces heavy drinking days compared to the active control. It also aims to investigate, using a 2 by 2 factorial (2x2) design, the hypothesis that the effects of the glutamate modulator are enhanced when combined with behavioral treatment.

The Role of Brief Potent Glutamatergic Modulation in Addressing Problem Drinking: a Randomized, Controlled Trial

The Role of Brief Potent Glutamatergic Modulation in Addressing Problem Drinking

Condition
Alcohol Use Disorder
Intervention / Treatment

-

Contacts and Locations

New York

NYSPI, New York, New York, United States, 10032

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Active alcohol use disorder, with at least 4 heavy drinking day over the past 7 days (greater than 4 drinks a day for males, greater than 3 drinks for females). In the case of the use of other drugs, alcohol is designated as the primary drug
  • 2. Physically healthy
  • 3. No adverse reactions to study medications
  • 4. 21-70 years of age
  • 5. Capacity to consent and comply with study procedures, including sufficient proficiency in English
  • 6. Seeking to reduce or stop alcohol use
  • 1. Meets DSM IV criteria for current major depression, bipolar disorder, schizophrenia, or any psychotic illness, including substance-induced psychosis
  • 2. Physiological dependence on another substance, such as opioids or benzodiazepines, excluding caffeine, nicotine, and cannabis
  • 3. Delirium, Dementia, Amnesia, Cognitive Disorders, or Dissociative disorders
  • 4. Current suicide risk or a history of suicide attempt within the past year
  • 5. Inability to safely initiate 24 hours of abstinence from alcohol, as evidenced by CIWA greater than 10 during screening; history of severe withdrawal phenomena over the past 6 months (e.g., inpatient stabilization, withdrawal-related seizure); or self-reported inability to maintain abstinence for 24 hours.
  • 6. Pregnant or interested in becoming pregnant during the study period
  • 7. Any of the following cardiac conditions: clinically significant left ventricular hypertrophy, angina, clinically significant arrhythmia, or mitral valve prolapse
  • 8. Unstable physical disorders which might make participation hazardous such as hypertension (\>160/90), anemia, active hepatitis or other liver disease (transaminase levels \< 2-3 X the upper limit of normal will be considered acceptable), epilepsy, or untreated diabetes. Participants reporting HIV+ status will be asked to provide information about their current treatment, including all medications. Participants who are on the antiretroviral ritonavir (Norvir) will be excluded due to the possibility that study medications in combination with this medication may increase the risk of drug-induced hepatitis.
  • 9. Previous history of misuse or abuse of study medications, and a history of an adverse reaction/experience with prior exposure to study medications
  • 10. Recent history of significant violance
  • 11. On psychotropic or other medications whose effect could be disrupted by participation in the study

Ages Eligible for Study

21 Years to 70 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

New York State Psychiatric Institute,

Elias Dakwar, MD, PRINCIPAL_INVESTIGATOR, NYSPI/Columbia

Study Record Dates

2024-08-31