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A Multimodal Neuroimaging Study of Brain Activation Patterns Under Ketamine

Primary Purpose

Major Depressive Disorder

Status
Completed
Phase
Early Phase 1
Locations
Study Type
Interventional
Intervention
Ketamine
Placebo
Sponsored by
Psychiatric University Hospital, Zurich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Major Depressive Disorder

Eligibility Criteria

20 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • treatment resistant depressive episode
  • no restrictions regarding antidepressant medication

Exclusion Criteria:

  • lifetime antidepressant treatment with ketamine
  • lifetime recreational use of ketamine
  • cardiovascular diseases such as hypertonia, cardiac insufficiency or myocardial infarct in the past six months
  • insufficiently treated anemia
  • hyper- or hypothyroidism
  • lifetime increased intracranial pressure or glaucoma
  • chronic physical diseases
  • hepatorenal dysfunction
  • any relevant psychiatric or neurological comorbidity, in particular dementia, epileptic seizures (lifetime), schizophrenia (lifetime), psychosis (lifetime), or post-traumatic stress disorder (current).
  • acute suicidality
  • substance abuse disorders
  • recent heart or head surgery
  • metallic body implants
  • agoraphobia
  • pregnancy
  • left handedness

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    Ketamine

    Placebo

    Arm Description

    i.v. infusion of 0.25 mg/kg S-ketamine over 40 min

    i.v. infusion of NaCl over 40 min

    Outcomes

    Primary Outcome Measures

    Change in functional reactivity to emotional stimuli
    fMRI BOLD
    Change in glutamate concentrations in prefrontal cortex
    1H-MRS
    Change in resting-state functional connectivity
    rsfMRI

    Secondary Outcome Measures

    Full Information

    First Posted
    July 13, 2018
    Last Updated
    March 19, 2019
    Sponsor
    Psychiatric University Hospital, Zurich
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03609190
    Brief Title
    A Multimodal Neuroimaging Study of Brain Activation Patterns Under Ketamine
    Official Title
    Brain Activation Patterns Under Emotional and Neurochemic Stimulation With Ketamine: A Multimodal Neuroimaging Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2019
    Overall Recruitment Status
    Completed
    Study Start Date
    January 2015 (Actual)
    Primary Completion Date
    December 2018 (Actual)
    Study Completion Date
    December 2018 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Psychiatric University Hospital, Zurich

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The aim of the project is to establish a multimodal imaging approach for the investigation of the neural mechanisms underlying neuroreceptor regulation, glutamatergic metabolism and brain function that are of particular relevance for major depressive disorder (MDD) and that can be translated into clinical applications. There is growing evidence for imbalance with regard to glutamatergic neurotransmission in stress-related affective disorders. Further support for the hypothesis that dysfunctional glutamatergic signaling underlies major depressive disorder, and indeed that its reversal constitutes a potential efficacious mechanism of action, is provided by the evidence that pharmacological compounds active at the N-methyl-D-aspartate (NMDA) ionotropic glutamate receptor such as ketamine exert rapid antidepressant effects. As a tool compound ketamine enables the safe investigation of the brain region-specific effects of NMDA receptor antagonism in terms of glutamatergic neurotransmission, brain function and the association of these neural changes with emotional state, thereby allowing for increased understanding of the therapeutic mechanism of action. The possibility to simultaneously study brain perfusion (arterial spin labeling), functional brain activity (fMRI) and connectivity (resting state fMRI), neurometabolism (proton magnetic resonance spectroscopy) and metabotropic glutamate receptor densities (positron emission tomography) will unravel their functional interplay in the mechanisms underlying the regulation of mood and cognition. Combining those imaging modalities with treatment interventions in healthy subjects and depressed patients, this project aims at providing insight into the neuropharmacological effects of ketamine and its antidepressant properties.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Major Depressive Disorder

    7. Study Design

    Primary Purpose
    Basic Science
    Study Phase
    Early Phase 1
    Interventional Study Model
    Crossover Assignment
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    10 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Ketamine
    Arm Type
    Experimental
    Arm Description
    i.v. infusion of 0.25 mg/kg S-ketamine over 40 min
    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    i.v. infusion of NaCl over 40 min
    Intervention Type
    Drug
    Intervention Name(s)
    Ketamine
    Intervention Description
    i.v. infusion of 0.25 mg/kg S-ketamine over 40 min
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Intervention Description
    i.v. infusion of NaCl over 40 min
    Primary Outcome Measure Information:
    Title
    Change in functional reactivity to emotional stimuli
    Description
    fMRI BOLD
    Time Frame
    Change from baseline to 24h-post infusion
    Title
    Change in glutamate concentrations in prefrontal cortex
    Description
    1H-MRS
    Time Frame
    Change from baseline to 24h-post infusion
    Title
    Change in resting-state functional connectivity
    Description
    rsfMRI
    Time Frame
    Change from baseline to 24h-post infusion

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    20 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: treatment resistant depressive episode no restrictions regarding antidepressant medication Exclusion Criteria: lifetime antidepressant treatment with ketamine lifetime recreational use of ketamine cardiovascular diseases such as hypertonia, cardiac insufficiency or myocardial infarct in the past six months insufficiently treated anemia hyper- or hypothyroidism lifetime increased intracranial pressure or glaucoma chronic physical diseases hepatorenal dysfunction any relevant psychiatric or neurological comorbidity, in particular dementia, epileptic seizures (lifetime), schizophrenia (lifetime), psychosis (lifetime), or post-traumatic stress disorder (current). acute suicidality substance abuse disorders recent heart or head surgery metallic body implants agoraphobia pregnancy left handedness

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    33309459
    Citation
    Herrera-Melendez A, Stippl A, Aust S, Scheidegger M, Seifritz E, Heuser-Collier I, Otte C, Bajbouj M, Grimm S, Gartner M. Gray matter volume of rostral anterior cingulate cortex predicts rapid antidepressant response to ketamine. Eur Neuropsychopharmacol. 2021 Feb;43:63-70. doi: 10.1016/j.euroneuro.2020.11.017. Epub 2020 Dec 11.
    Results Reference
    derived
    PubMed Identifier
    30819549
    Citation
    Gartner M, Aust S, Bajbouj M, Fan Y, Wingenfeld K, Otte C, Heuser-Collier I, Boker H, Hattenschwiler J, Seifritz E, Grimm S, Scheidegger M. Functional connectivity between prefrontal cortex and subgenual cingulate predicts antidepressant effects of ketamine. Eur Neuropsychopharmacol. 2019 Apr;29(4):501-508. doi: 10.1016/j.euroneuro.2019.02.008. Epub 2019 Feb 26.
    Results Reference
    derived

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    A Multimodal Neuroimaging Study of Brain Activation Patterns Under Ketamine

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