A Multimodal Neuroimaging Study of Brain Activation Patterns Under Ketamine

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.

Intervention / Treatment

  • Ketamine (DRUG)
    i.v. infusion of 0.25 mg/kg S-ketamine over 40 min
  • Placebo (DRUG)
    i.v. infusion of NaCl over 40 min

Condition or Disease

  • Major Depressive Disorder

Phase

  • Early Phase 1
  • Study Design

    Study type: INTERVENTIONAL
    Status: Completed
    Study results: No Results Available
    Age: 20 Years to 60 Years
    Enrollment: 10 (ACTUAL)
    Funded by: Other
    Allocation: Randomized
    Primary Purpose: Basic Science

    Masking

    QUADRUPLE:
    • Participant
    • Care Provider
    • Investigator
    • Outcomes Assessor

    Clinical Trial Dates

    Start date: Jan 01, 2015 ACTUAL
    Primary Completion: Dec 01, 2018 ACTUAL
    Completion Date: Dec 01, 2018 ACTUAL
    Study First Posted: Aug 01, 2018 ACTUAL
    Results First Posted: Aug 31, 2020
    Last Updated: Mar 19, 2019

    Sponsors / Collaborators

    Responsible Party: Milan Scheidegger

    Participant Groups

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

    • i.v. infusion of NaCl over 40 min

    Eligibility Criteria

    Sex: All
    Minimum Age: 20
    Maximum Age: 60
    Age Groups: Adult
    Healthy Volunteers: Yes

    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

    Primary Outcomes
    • fMRI BOLD

    • 1H-MRS

    • rsfMRI

    More Details

    NCT Number: NCT03609190
    Other IDs: E-31/2008
    Study URL: https://clinicaltrials.gov/study/NCT03609190
    Last updated: Sep 29, 2023