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
About this trial
This is an interventional basic science trial for Major Depressive Disorder
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
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
NCT ID
NCT03609190
First Posted
July 13, 2018
Last Updated
March 19, 2019
Sponsor
Psychiatric University Hospital, Zurich
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
Learn more about this trial
A Multimodal Neuroimaging Study of Brain Activation Patterns Under Ketamine
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