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.
Study Design
Study type: | INTERVENTIONAL |
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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 |
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Clinical Trial Dates
Start date: | Jul 01, 2013 | |
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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
Location
Participant Groups
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Healthy participants will receive ketamine in the scan
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Depressed participants will receive ketamine in the scan
Eligibility Criteria
Sex: | All |
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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.
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
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Glutamate Metabolism 40-75 minutes
More Details
NCT Number: | NCT02037035 |
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Other IDs: | 1305011972 |
Study URL: | https://clinicaltrials.gov/study/NCT02037035 |
Last updated: Sep 29, 2023