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NCT Number: NCT06213324

Neural Circuit Effects of Ketamine in Depression

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.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Icahn School of Medicine at Mount Sinai

New York, 10029, United States

Location status: Recruiting

Location contact

James Murrough, MD, PhD

PRINCIPAL_INVESTIGATOR

Sibilla Masieri

CONTACT

[email protected],

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

ketamine

Drug

0.5 mg/kg ketamine dissolved in 100 mL saline, delivered intravenously

Placebo

Drug

Normal saline delivered intravenously

Primary outcomes

  1. sgACC response to the Incentive Flanker Task

    Time frame: Baseline

    Subgenual anterior cingulate cortex (sgACC) response to reward measured by the BOLD (Blood Oxygen Level Dependent) signal within the sgACC region of the brain, during an fMRI Incentive Flanker Task in healthy controls and in adults with MDD. BOLD signal is the unit of measure of this outcome.

Secondary outcomes

  1. Treatment-related change in sgACC response to the Incentive Flanker Task

    Time frame: Baseline and Day 1

    Treatment-related change from baseline to 1-day post treatment in subgenual anterior cingulate cortex (sgACC) response to reward measured by the BOLD (Blood Oxygen Level Dependent) signal within the sgACC region of the brain, during an fMRI Incentive Flanker Task. MDD adults only.

Study contacts

Contact information is provided by the study sponsor or research team.

Sibilla Masieri

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

Icahn School of Medicine at Mount Sinai

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Official study title

Neural Circuit-Specific Mechanisms of Ketamine's Effect on Anhedonia and Anxiety in Depression Using Ultra-High Field 7-Tesla MRI

Important dates

Study start
2024
Primary completion
2028
Study completion
2028
First posted
Jan 19, 2024
Registry last updated
Jul 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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