Naltrexone Plus Ketamine for the Rapid Treatment of Major Depressive Disorder and Alcohol Use Disorder
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ClinicalTrials.gov Identifier: NCT03658330 |
Recruitment Status :
Completed
First Posted : September 5, 2018
Last Update Posted : September 7, 2018
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Condition or disease | Intervention/treatment | Phase |
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Major Depressive Disorder Alcohol Use Disorder | Drug: Ketamine + Naltrexone | Phase 2 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 5 participants |
Allocation: | N/A |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Naltrexone Plus Ketamine for the Rapid Treatment of Major Depressive Disorder and Alcohol Use Disorder |
Actual Study Start Date : | May 2016 |
Actual Primary Completion Date : | October 2016 |
Actual Study Completion Date : | June 2018 |
Arm | Intervention/treatment |
---|---|
Experimental: Ketamine + Naltrexone
Subjects will receive (1) intravenous ketamine (0.5 mg/kg) once a week for 4 weeks (a total of 4 infusions) and (2) intramuscular naltrexone (380 mg) once a month (a total of 1 injection).
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Drug: Ketamine + Naltrexone
Subjects will receive (1) intravenous ketamine (0.5 mg/kg) once a week for 4 weeks (a total of 4 infusions) and (2) intramuscular naltrexone (380 mg) once a month (a total of 1 injection). |
- Response in symptoms of depression as measured by the Montgomery-Asberg Depression Rating Scale (MADRS) [ Time Frame: Day 21 ]Response is defined as a ≥ 50% improvement from baseline in MADRS scores. The MADRS has a total range of 0-60. Higher scores represent a worse outcome (i.e., more depression).
- Obsessive Compulsive Drinking Scale (OCDS) [ Time Frame: Day 21 ]The Obsessive Compulsive Drinking Scale is designed to assess alcohol craving and consumption. The scale has a total score range of 0-56. Higher scores represent a worse outcome (i.e., more alcohol problems).

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Ages Eligible for Study: | 21 Years to 65 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Male or female, 21-65 years old
- Current major depressive disorder without psychotic features by DSM-5
- Montgomery-Åsberg Depression Rating Scale (MADRS) ≥ 20
- Current alcohol use disorder by DSM-5
- Heavy drinking at least 3 times in the past month ('heavy drinking' defined as ≥ 5 standard drinks per day for men and ≥ 4 standard drinks per day for women)
- Abstinence from alcohol drinking for > 5 days prior to ketamine infusion
- Able to provide written informed consent
Exclusion Criteria:
- Current substance use disorder by DSM-5 in the past 3 months (except alcohol, tobacco, or cannabis)
- Current or past history of psychotic features or psychotic disorder
- Current or past history of delirium or dementia
- Current uncontrolled hypertension (systolic BP > 170 mm Hg or diastolic BP > 100 mm Hg)
- Unstable medical condition or allergy to ketamine, naltrexone, or lorazepam---clinically determined by a physician
- Imminent suicidal or homicidal risk
- Pregnant or nursing women, positive pregnancy test, or inadequate birth control methods in women of childbearing potential
- Positive opioid or illicit drug screen test (except marijuana)
- Opioid use within 10 days prior to study medication (injectable naltrexone) or risks for opioid use during the study
- Liver enzymes that are three times higher than the upper limit of normal

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03658330
Principal Investigator: | Gihyun Yoon, MD | VA Connecticut Healthcare System |
Responsible Party: | Gihyun Yoon, Principal Investigator, VA Connecticut Healthcare System |
ClinicalTrials.gov Identifier: | NCT03658330 |
Other Study ID Numbers: |
GY0004 |
First Posted: | September 5, 2018 Key Record Dates |
Last Update Posted: | September 7, 2018 |
Last Verified: | September 2018 |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Ketamine Naltrexone Depression Alcohol |
Disease Alcoholism Depressive Disorder Depression Depressive Disorder, Major Alcohol Drinking Pathologic Processes Mood Disorders Mental Disorders Behavioral Symptoms Drinking Behavior Alcohol-Related Disorders Substance-Related Disorders Chemically-Induced Disorders Naltrexone |
Ketamine Analgesics Sensory System Agents Peripheral Nervous System Agents Physiological Effects of Drugs Anesthetics, Dissociative Anesthetics, Intravenous Anesthetics, General Anesthetics Central Nervous System Depressants Excitatory Amino Acid Antagonists Excitatory Amino Acid Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Alcohol Deterrents |