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CompletedEarly Phase 1

Examining The Effect Of Ketamine On Glutamate/Glutamine Cycling

NCT02037035 · Yale University

Closed to entry
Status
Not accepting participants
Early Phase 1
Phase
36
Target enrolment
1
Study sites
1 US states

What it is testing

Summary

This study is looking at the mechanisms underlying the behavioral effects of ketamine in healthy and depressed individuals.

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • Glutamate Metabolism

    Measured over 40-75 minutes

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

21 Years to 65 Years
Ages
All
Sex
Accepted
Healthy volunteers
Healthy Group Inclusion Criteria: * Male or female between the ages of 21-65 years. * Able to provide written informed consent. * Able to read and write English. Exclusion Criteria: * Personal or first-degree family member with history of mood, anxiety, or psychotic axis I DSM-IV disorders confirmed after comprehensive psychiatric evaluation. * Any history of serious medical or neurological illness. * Any signs of major medical or neurological illness on examination or as a result of ECG screening or laboratory studies. * Lifetime history of psychoactive substance or alcohol dependence or substance or alcohol abuse (other than nicotine or caffeine abuse), or drinking more that 5 drinks/week during the last year. * Abnormality on physical examination. * A positive pre-study (screening) urine drug screen or, at the study physician's discretion on any drug screens given before the scans. * Pregnant or lactating women or a positive urine pregnancy test for women of child-bearing potential at screening or prior to any imaging day. * Subjects who test positive for HIV or viral hepatitis (hepatitis B and/or C) * Has received either prescribed or over-the-counter (OTC) centrally active medicine or herbal supplements within the week prior to the MRI scan. * Any history indicating learning disability, mental retardation, or attention deficit disorder. * Known sensitivity to ketamine. * Body circumference of 52 inches or greater. * Body weight of 280 pounds or greater. * History of claustrophobia. * Presence of cardiac pacemaker or other electronic device or ferromagnetic metal foreign bodies in vulnerable positions as assessed by a standard pre-MRI screening questionnaire. * Donation of blood in excess of 500 mL within 56 days prior to dosing. * History of sensitivity to heparin or heparin-induced thrombocytopenia. * Resting blood pressure lower than 90/60 or higher than 150/90,or resting heart rate lower than 45/min or higher than 100/min. Depression Group Inclusion Criteria: * Male or female between the ages of 21-65 years. * Able to provide written informed consent. * Current MDD Single Episode (296.2x) or Recurrent (296.3x), as determined by the Structured Clinical Interview for DSM-IV (SCID) patient edition * Montgomery Asberg Depression Rating Scale (MADRS) score of 18 or higher at baseline and start of first 13C-MRS. * Quick Inventory of Depressive Symptoms - Self-Report (QIDS-SR16) score of 19 or higher at baseline and start of first 13C-MRS. * No psychotropic medications for 2 or more weeks (4 weeks for Fluoxetine) prior to first 13C-MRS. * Be able to understand and speak English. Exclusion Criteria: * Patients with a history of DSM-IV-TR diagnosis of bipolar disorder or schizophrenia or schizoaffective disorder or currently exhibiting psychotic features associated with their depression; dementia or suspicion thereof, is also exclusionary. * First-degree family member with history of schizophrenia or any other psychotic disorder. * Serious suicide or homicide risk, as assessed by evaluating clinician; A serious suicide risk will be considered an inability to control suicide attempts, imminent risk of suicide in the investigator's judgment, or a history of serious suicidal behavior, which is defined using the Columbia-Suicide Severity Rating Scale (C-SSRS) as either (1) one or more actual suicide attempts in the 3 years before study entry with the lethality rated at 3 or higher, or (2) one or more interrupted suicide attempts with a potential lethality judged to result in serious injury or death. * Substance abuse or dependence during the 12 months prior to screening. * Any history of serious medical or neurological illness. * Any signs of major medical or neurological illness. * Abnormality on physical examination. A subject with a clinical abnormality may be included only if the study physician considers the abnormality will not introduce additional risk factors and will not interfere with the study procedure. * A positive pre-study (screening) urine drug screen or on any drug screens given before the scans. * Pregnant or lactating women or a positive urine pregnancy test for women of childbearing potential at screening or prior to any imaging day. * Any history indicating learning disability, or mental retardation. * Known sensitivity to ketamine. * Body weight of 280 pounds or greater. * History of claustrophobia. * Presence of cardiac pacemaker or other electronic device or ferromagnetic metal foreign bodies in vulnerable positions as assessed by a standard pre-MRI screening questionnaire. * Donation of blood in excess of 500 mL within 56 days prior to dosing. * History of sensitivity to heparin or heparin-induced thrombocytopenia. * Resting blood pressure lower than 90/60 or higher than 150/90,or resting heart rate lower than 45/min or higher than 100/min.

Where

1 study site

FacilityCityRegionCountry
Yale Depression Research ProgramNew HavenConnecticutUnited States

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT02037035 on ClinicalTrials.gov →

Last updated in the registry 2021-09-08. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits