Actively Recruiting

Early Phase 1
Age: 25Years - 65Years
All Genders
NCT06788249

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

Age: 25Years - 65Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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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