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RecruitingPhase 4

Neural Circuit Effects of Ketamine in Depression

NCT06213324 · Icahn School of Medicine at Mount Sinai

Recruiting
Status
Accepting participants
Phase 4
Phase
120
Target enrolment
1
Study sites
1 US states

What it is testing

Summary

This project is designed to examine the role of the subgenual anterior cingulate cortex (sgACC) in anhedonia and anxiety in humans with depression, as well as the acute and sustained effects of ketamine on agACC activation and depression symptoms.

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

  • sgACC response to the Incentive Flanker Task

    Measured over Baseline

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

18 Years to 65 Years
Ages
All
Sex
Accepted
Healthy volunteers
Inclusion Criteria: MDD Group * Male or female aged 18-65 years; * Ability for participant to comply with the requirements of the study as determined by the PI; * Capacity to provide informed consent; * Meets diagnostic criteria for current MDD according to the Diagnostic and Statistical Manual of Mental Disorders-Fifth Edition (DSM-5); * In a current major depressive episode (MDE) of at least moderate severity according to DSM-5; * Women must be using a medically accepted reliable means of contraception (if using an oral contraceptive medication, they must also be using a barrier contraceptive) or not be of childbearing potential (i.e., surgically sterile, postmenopausal for at least one year). * Women of childbearing potential must have a negative pregnancy test at screening and prior to the infusion. HC Group * Male or female aged 18-65 years; * Capacity to provide informed consent; * Women must be using a medically accepted reliable means of contraception (if using an oral contraceptive medication, they must also be using a barrier contraceptive) or not be of childbearing potential (i.e., surgically sterile, postmenopausal for at least one year). * Ability for participant to comply with the requirements of the study as determined by the PI; Exclusion Criteria: MDD Group * Current or history of schizophrenia or other psychotic disorder/episode, bipolar disorder, neurodevelopmental disorder, or neurocognitive disorder; * Current major depressive disorder with psychotic features; * Substance use disorder within the past 2 years\*; * Lifetime history of ketamine use disorder; * Antidepressant medication within 2 weeks of Baseline (4 weeks for fluoxetine); * Severe current illness as reflected by a CGI score \>5; * Any unstable medical illnesses including hepatic, renal, gastroenterologic, respiratory, cardiovascular (including ischemic heart disease); endocrinologic, neurologic (including history of severe head injury), immunologic, or hematologic disease; * Clinically significant abnormalities of laboratories, physical examination, or ECG; * Positive urine toxicology screen for drugs of abuse at the time of screening, except cannabis; * Women who plan to become pregnant, are pregnant or are breast-feeding (because the medical risk of using ketamine during pregnancy and breast-feeding is unknown); * Active suicidal intent or plan; CSSRS score \>2; * Any contraindications to MRI, including claustrophobia, any trauma or surgery which may have left magnetic material in the body, magnetic implants or pacemakers, and inability to lie still for 1 hour or more; * Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the participant or the quality of the data. HC Group * Current or history of any psychiatric, neurodevelopmental disorder, or neurocognitive disorder; * Substance use disorder within the past 2 years\*; * Any unstable medical illnesses including hepatic, renal, gastroenterologic, respiratory, cardiovascular (including ischemic heart disease); endocrinologic, neurologic (including history of severe head injury), immunologic, or hematologic disease; * Clinically significant abnormalities of laboratories or physical examination; * Positive urine toxicology screen for drugs of abuse at the time of screening, except cannabis; * Current pregnancy; * Women who are breast feeding; * Active suicidal intent or plan; CSSRS score \>2; * Any contraindications to MRI, including claustrophobia, any trauma or surgery which may have left magnetic material in the body, magnetic implants or pacemakers, and inability to lie still for 1 hour or more.

Where

1 study site

FacilityCityRegionCountry
Icahn School of Medicine at Mount SinaiNew YorkNew YorkUnited States

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.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT06213324 on ClinicalTrials.gov →

Last updated in the registry 2025-07-03. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits