Brain scans reveal how ketamine works in stubborn bipolar depression
NCT ID NCT06620042
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at how ketamine affects brain connections in people with bipolar depression that hasn't improved with other treatments. Twenty adults received ketamine and had brain scans before and after. The goal was to see if changes in brain activity could predict who gets better.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ketamine
- What this could lead to
- If successful, this could help identify brain changes that predict who will respond to ketamine, potentially guiding more personalized treatment for bipolar depression.
- What could go wrong
- This is a small, early-phase study with only 20 participants and no placebo group. The results may not apply to everyone, and the brain scan findings may not lead to clear clinical benefits.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
20 people
The number who actually took part.
- Started
-
Nov 2024
- Finished
-
Oct 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 75 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Written informed consent before any study related procedures are performed 2. Males/females at least 18 years of age but no older than 75 years of age 3. Meet DSM-5 criteria for a current Major Depressive Episode and lifetime Bipolar I disorder or Bipolar II disorder as determined by both: A. a clinician's diagnostic evaluation and B. confirmed with the MINI International Neuropsychiatric Interview (MINI 7.0.2) 4. A current depressive episode that has lasted a minimum of 4 weeks as determined by both: A. a clinician's diagnostic evaluation and B. confirmed with the MINI International Neuropsychiatric Interview (MINI 7.0.2) 5. Meet all the following criteria on symptom rating scales at screening: A. Montgomery Asberg Depression Rating Scale (MADRS) score ≥20 B. Young Mania Rating Scale (YMRS) score of ≤ 5 C. QIDS-SR-16 score of ≥ 11 6. Have had ≥ 2 adequate trials of mood stabilizers, antipsychotics (only those FDA approved for bipolar depression), or antidepressants or augmentation strategies during their lifetime. An adequate trial is defined as 4 weeks of medication at the minimum FDA approved dose. 7. In the opinion of the investigator, the patient is willing and able to comply with scheduled visits, treatment plan, and other trial procedures for the duration of the study. Exclusion Criteria: 1. Meet DSM-5 criteria for schizophrenia, schizophreniform disorder, schizoaffective disorder, mental retardation, or pervasive developmental disorder 2. Meets any exclusion criteria for ketamine treatment (uncontrolled arterial hypertension, uncontrolled hyperthyroidism, severe ischemic heart disease or heart failure, severe liver or kidney disease, space occupying lesion in the brain or the spinal cord, and uncontrolled glaucoma) 3. The patient is pregnant or breast feeding 4. The patient has a severe medical illness or severe neurological disorder 5. The patient has a known ketamine allergy or is taking a medication that may significantly interact with ketamine (see Appendix) 6. Diagnosis of psychotic features during the current depressive episode or within the past 6 months 7. Was previously enrolled in the trial 8. Active moderate or severe substance use disorder within the last 3 months (no exclusion for tobacco use disorder of any severity) 9. Current episode of mania/hypomania or mixed episode according to MINI or study clinician 10. MRI contraindications * Severe head trauma * Claustrophobia incompatible with scanning * Cardiac pacemaker * Implanted cardiac defibrillator * Aneurysm brain clip * Inner ear implant * Prior history as a metal worker and/or certain metallic objects in the body -- must complete MRI screening form and be approved by MRI technologist before each scan * History of clinically significant vertigo middle ear disorder, or double vision
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Cleveland Clinic Lutheran Hospital
Cleveland, Ohio, 44113, United States
-
Cleveland Clinic Lutheran Hospital
Ohio City, Ohio, 44113, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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