CompletedEarly Phase 1ketamine
Examining The Effect Of Ketamine On Glutamate/Glutamine Cycling
Sponsored by Yale University
NCT ID
NCT02037035
Target Enrollment
36 participants
Start Date
2013-07
Est. Completion
2021-06
About This Study
This study is looking at the mechanisms underlying the behavioral effects of ketamine in healthy and depressed individuals.
Conditions Studied
Interventions
- •Ketamine
Eligibility
Age:21 Years - 65 Years
Healthy Volunteers:Yes
View full eligibility criteria
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.
Study Locations (1)
Yale Depression Research Program
New Haven, Connecticut, United States