Status:
NOT_YET_RECRUITING
Understanding the Role of the Kappa Opioid Receptor in Ketamine's Attenuation of Suicidal Thoughts
Lead Sponsor:
New York State Psychiatric Institute
Collaborating Sponsors:
American Foundation for Suicide Prevention
Conditions:
Major Depressive Disorder (MDD)
Eligibility:
All Genders
18-59 years
Phase:
PHASE4
Brief Summary
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 ba...
Eligibility Criteria
Inclusion
- DSM5 unipolar major depressive episode
- Persons of child-bearing potential must agree to use an acceptable method of birth control throughout the study.
Exclusion
- Current or past ketamine abuse or dependence ever (lifetime)
- Any medical contraindication to ketamine, including prior ineffective trial of or medically significant adverse reaction to ketamine.
- 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.
- 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).
- 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.
- 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.
- 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.
- Use of more than incidental NSAIDs (including aspirin), anti-inflammatories, immune suppressants or other pain medications.
- 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.
- Lacks capacity to consent
- Aggressive behavior that is a significant threat to others such as physically assaultive behavior (in the last month).
- Pregnancy, abortion or miscarriage in the previous two months or plans to conceive during the course of study participation.
- Currently lactating
- 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.
- Any condition or material in the body that is a contraindication for MRI procedures.
- Current, past or anticipated exposure to radiation except if the exposure was at our PET center where the precise exposure is known
- ECT within past 6 months
- 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
- Blind or with visual impairment that cannot be corrected with corrective lenses (glasses or contact lenses)
- No emergency contact
Key Trial Info
Start Date :
February 1 2026
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 30 2027
Estimated Enrollment :
12 Patients enrolled
Trial Details
Trial ID
NCT07139106
Start Date
February 1 2026
End Date
September 30 2027
Last Update
September 19 2025
Active Locations (1)
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1
New York State Psychiatric Institute
New York, New York, United States, 10032