Examining The Effect Of Ketamine On Glutamate/Glutamine Cycling

Brief Summary

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

Intervention / Treatment

  • Ketamine (DRUG)
    N/A

Condition or Disease

  • Depression

Phase

  • Early Phase 1
  • Study Design

    Study type: INTERVENTIONAL
    Status: Completed
    Study results: No Results Available
    Age: 21 Years to 65 Years
    Enrollment: 36 (ACTUAL)
    Funded by: Other|NIH
    Allocation: Non-Randomized
    Primary Purpose: Basic Science

    Masking

    SINGLE:
    • Participant

    Clinical Trial Dates

    Start date: Jul 01, 2013
    Primary Completion: Jun 01, 2021 ACTUAL
    Completion Date: Jun 01, 2021 ACTUAL
    Study First Posted: Jan 15, 2014 ESTIMATED
    Results First Posted: Aug 31, 2020
    Last Updated: Sep 07, 2021

    Sponsors / Collaborators

    Lead Sponsor: Yale University
    Lead sponsor is responsible party
    Responsible Party: N/A

    Participant Groups

    • Healthy participants will receive ketamine in the scan

    • Depressed participants will receive ketamine in the scan

    Eligibility Criteria

    Sex: All
    Minimum Age: 21
    Maximum Age: 65
    Age Groups: Adult / Older Adult
    Healthy Volunteers: Yes

    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.

    Primary Outcomes
    • Glutamate Metabolism 40-75 minutes

    More Details

    NCT Number: NCT02037035
    Other IDs: 1305011972
    Study URL: https://clinicaltrials.gov/study/NCT02037035
    Last updated: Sep 29, 2023