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CompletedEarly Phase 1

A Multimodal Neuroimaging Study of Brain Activation Patterns Under Ketamine

NCT03609190 · Psychiatric University Hospital, Zurich

Closed to entry
Status
Not accepting participants
Early Phase 1
Phase
10
Target enrolment
Study sites

What it is testing

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.

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • Change in functional reactivity to emotional stimuli

    Measured over Change from baseline to 24h-post infusion

  • Change in glutamate concentrations in prefrontal cortex

    Measured over Change from baseline to 24h-post infusion

  • Change in resting-state functional connectivity

    Measured over Change from baseline to 24h-post infusion

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

20 Years to 60 Years
Ages
All
Sex
Accepted
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

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

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NCT03609190 on ClinicalTrials.gov →

Last updated in the registry 2019-03-20. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits