Actively Recruiting
Pilot Study: Establishing Glutamatergic Changes in Rapid Antidepressant Effects of Ketamine
Led by University of Pennsylvania · Updated on 2026-04-21
10
Participants Needed
1
Research Sites
19 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
In the treatment of Major Depressive Disorder (MDD), ketamine can produce rapid but short-lasting improvements in mood. In order to develop a new generation of treatments with rapid and sustained efficacy, a better understanding of the mechanism of action is urgently needed. One candidate mechanism is the modulation of synaptic strength mediated by glutamatergic activity as ketamine has been suggested to increase synaptic strength. Although determining how ketamine impacts the glutamatergic system is essential to isolating its mechanism of action, the invasive nature of most assessment methods has limited our ability to do so in humans. The proposed research aims to determine if changes in glutamatergic activity, reflecting the modulation of synaptic strength, underlie the antidepressant effects of ketamine. In this project, the investigators will utilize a novel measure of glutamate imaging, GluCEST, to assess changes in glutamatergic activity to assess synaptic strength following ketamine administration. Ten individuals (aged 25-65) with a DSM-V diagnosis of MDD will undergo baseline GluCEST imaging prior to and following ketamine infusion. Both clinician-administered and subjective mood measures will be collected. It is predicted that ketamine will improve mood and increase glutamatergic activity and synaptic strength. Results from this project have the potential to identify the modifiable mechanisms by which rapid antidepressants work which could ultimately stimulate the development of novel interventions that work through the modulation of glutamatergic activity.
CONDITIONS
Official Title
Pilot Study: Establishing Glutamatergic Changes in Rapid Antidepressant Effects of Ketamine
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 25 and 65 years
- Current depression diagnosed by Structured Clinical Interview for DSM-V (SCID)
- Treatment-resistant depression with failure of at least two antidepressant or mood stabilizing treatments during current episode
- Able to understand and complete questionnaires in English
- Able to provide informed consent and pass a comprehension test about ketamine and study objectives
You will not qualify if you...
- Sleep disorders other than insomnia
- History of bipolar disorder, delirium, dementia, amnestic disorder, schizophrenia, or other psychotic disorders
- Alcohol or drug abuse within the past year
- Current smoker
- Significant medical or neurological illness affecting brain function or participation
- History of head trauma with significant loss of consciousness
- Metallic implants, pacemakers, tattoos, or MRI contraindications
- Claustrophobia or intolerance to MRI scanner environment
- Pregnancy in women
- Untreated hypertension
- Body mass index over 40
- Current prescription of 4 mg or more lorazepam equivalents daily or morning benzodiazepine dosing
- Currently receiving ECT, transcranial magnetic stimulation, vagal nerve stimulation, or deep brain stimulation
- Use of MAO inhibitors within two weeks prior to study drug
- Use of CYP3A4 inducers carbamazepine or modafinil within two weeks prior to and 24 hours after study drug
- Current use of Naltrexone
- Developmental delay, intellectual disability
- Diagnosis of delirium or encephalopathy within the past 12 months
- Prior participation in ketamine studies for depression
- Prior treatment or recreational use of ketamine
AI-Screening
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Trial Site Locations
Total: 1 location
1
University of Pennsylvania
Philadelphia, Pennsylvania, United States, 19104
Actively Recruiting
Research Team
J
Jennifer R Goldschmied, PhD
CONTACT
H
Holly Barilla, MS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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