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NCT07139106Not yet recruitingPhase 4

Understanding the Role of the Kappa Opioid Receptor in Ketamine's Attenuation of Suicidal Thoughts

Dynorphin/Kappa Opioid Receptor Signaling Role in Ketamine's Anti-suicidal Ideation Effect

Source: ClinicalTrials.gov · Last updated 3 Aug 2026

Brief summary (registry, in English)

This study explores how stress, suicidal thoughts, and ketamine's effects are connected in people with major depressive disorder. Stress increases the risk for suicidal thoughts, but the biological basis is unclear. Ketamine may help reduce suicidal thoughts by affecting stress-linked brain systems. This study will use smartphone tracking to monitor real-time responses to stress and positron emission tomography (PET) brain scans to study how ketamine affects brain pathways related to stress and suicidal thoughts in depressed individuals.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
12 (estimated)
First submitted
18 Aug 2025
Start date
1 Oct 2026
Primary completion date
1 Oct 2028
Lead sponsor
New York State Psychiatric Institute
Diseases
Depression
NCT number
NCT07139106

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 12
  • From 1 Oct 2026 to the primary completion date, 1 Oct 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Any medical contraindication to ketamine, including prior ineffective trial of or medically significant adverse reaction to ketamine.
  • Current or recent use of medications known to affect brain biology of interest such as competing for binding sites of PET tracer within 1 month.
  • Use of more than incidental NSAIDs (including aspirin), anti-inflammatories, immune suppressants or other pain medications.
  • Pregnancy, abortion or miscarriage in the previous two months or plans to conceive during the course of study participation.
  • Previous head injury with evidence of cognitive impairment. Subjects who endorse a history of prior head trauma and score 1.5 standard deviations below the mean on Trail-making A or B will be excluded from study participation.
  • Current, past or anticipated exposure to radiation except if the exposure was at our PET center where the precise exposure is known

Other illness

  • Clinically significant EKG abnormality in terms of ketamine administration (e.g., Ventricular tachycardia, evidence of myocardial ischemia, symptomatic bradycardia, unstable tachycardia, second degree (or greater) AV block).
  • Lifetime schizophrenia, schizoaffective illness, bipolar disorder, current psychotic depression; mild drug or alcohol use disorder in past 2 months; moderate or severe drug or alcohol use disorder in past 6 months; suicidal ideation with plan and/or intent within 6 months; suicide attempt in the past month.
  • Uncontrolled moderate or severe hypertension (≥160 mmHg systolic or ≥100 mmHg diastolic\[41\]), history of Raynaud's phenomenon, seizures, an open cut, sore, or bone fracture on or near the hands to be used for the cold pressor test.
  • Significant active physical illness, particularly if it may affect the brain biology being studied; including chronic pain syndrome and medically compromising eating disorders or epilepsy.
  • Any condition or material in the body that is a contraindication for MRI procedures.
  • Blind or with visual impairment that cannot be corrected with corrective lenses (glasses or contact lenses)

Lab values

  • For A-Line Subjects: Unstable relevant medical condition (i.e., condition not adequately stabilized for 3 months). Including bleeding disorders, the need to take medications that affect blood clotting, and certain platelet and hemoglobin cutoffs

Age

  • A first-degree family history of schizophrenia if the subject is less than 33 years old (mean age of onset for schizophrenia plus two standard deviations).

Other

  • Current or past ketamine abuse or dependence ever (lifetime)
  • Current or recent use of antidepressants within 14 days or benzodiazepines within 1 day. Use of fluoxetine or other long-acting antidepressant within 6 weeks.
  • Lacks capacity to consent
  • Aggressive behavior that is a significant threat to others such as physically assaultive behavior (in the last month).
  • Currently lactating
  • ECT within past 6 months
  • No emergency contact

Who the study is looking for

  • DSM5 unipolar major depressive episode
  • Persons of child-bearing potential must agree to use an acceptable method of birth control throughout the study.

Age in the registry: 18 years to 59 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
New York State Psychiatric Institute
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.