Ketamine Associated ACC GABA and Glutamate Change and Depression Remission:

Running, not enrolling · Early Phase 1

Conditions studied: Major Depressive Disorder, Treatment Resistant Depression, Bipolar Depression

In brief

This is a feasibility study and the goal of this project is to evaluate whether peak ACC GABA and glutamate, quantified as a CSF-corrected absolute concentration percent change from baseline, is associated with clinical remission, Montgomery Asberg Depression Rating Scale (MADRS) total score of \<10, to the anti-glutamatergic antidepressant ketamine. As MRS is expensive, we also aim to study a correlation between change in peripheral metabolites (GABA and glutamate) and central GABA and glutamate levels.

Key facts

Study ID

NCT03573349

Run by

Mayo Clinic

People needed

18

Starts

2019-01-03

Expected to finish

2026-12-01

Last updated by the study team

2026-07-02

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• For inclusion in this study, the following will be required:
• Ability to provide informed consent;
• Current psychiatric inpatient (voluntary only) or outpatient treatment;
• Male or female;
• Age 18-65 years;
• Meets diagnostic criteria for major depressive disorder/bipolar depression without psychotic features per the SCID DSM-IV-TR;
• PHQ-9 total score ≥ 15 at screening and at baseline (just prior to first acute phase ketamine infusion);
• Treatment-resistant depression (TRD), as defined by failure of at least two previous antidepressant treatments within the current depressive episode. Failed antidepressant treatments can include pharmacotherapy for depression at an adequate dose for at least 8 weeks, or an acute series of at least 6 administrations of electroconvulsive therapy (ECT) or an acute series of Transcranial magnetic stimulation (TMS);
• Ability to pass a comprehension assessment test related to effects of ketamine and trial objectives and criteria.
• Exclusion Criteria: Based on ketamine's known difficulties with the induction of perceptual/psychomimetic symptoms, the exclusion criteria for this study will be as follows:
• Inability to speak English
• Patients with a BMI >40.
• Any current psychiatric diagnosis other than anxiety disorders needing concurrent antidepressant therapy
• Personality disorder being the primary diagnosis
• Diagnosis of schizophrenia, schizoaffective disorder, post-traumatic stress disorder, or active psychotic symptoms;
• Ongoing prescription of > 4 mg lorazepam equivalents (total) daily, or morning dosing of any benzodiazepine at the time of assessment;
• Medications known to affect glutamate (i.e., riluzole, carbamazepine) or GABA (zaleplon, zolpidem, zopiclone, valproate, gabapentin, pregabalin, tiagabine, and vigabatrin) are prohibited within two weeks prior to administration of study drug;
• Antidepressant Monoamine Oxidase Inhibitors (MAOIs) are prohibited two weeks prior to the administration of the study drug.
• CYP3A4 inducers carbamazepine and modafinil are prohibited within two weeks prior to administration of the study drug and at least 24 hours after the last dose of study drug.
• Currently undergoing TMS, vagal nerve stimulation, or deep brain stimulation as either an acute or maintenance treatment of depression;
• ECT in the past 12 months;
• Any active or unstable medical condition judged by the study psychiatrist as conferring too great a level of medical risk to allow inclusion in the study;
• Use of methamphetamine, cocaine, or cannabis. Abuse of stimulant(s) within the prior 12 months;
• Any current substance use disorder (excluding nicotine and caffeine). Note: Persons will be allowed to enroll in this study if their substance use is in complete (not partial) and sustained (> 1 year) remission;
• History of traumatic brain injury that resulted in loss of consciousness;

Where it is running

• Mayo Clinic in Rochester — Rochester, Minnesota, United States

Full record on ClinicalTrials.gov

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