Ketamine shows promise for teen depression in small trial
NCT ID NCT05045378
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested whether low-dose ketamine infusions could quickly reduce depression in teenagers aged 13 to 19 whose depression had not improved with at least two other antidepressants. The trial was small, with only 12 participants, and compared ketamine to a placebo (midazolam). The goal was to see if ketamine could provide rapid relief for treatment-resistant depression in adolescents.
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 it works, this could point toward a fast-acting treatment option for teenagers with depression that hasn't responded to other medications.
- What could go wrong
- This is a very small, early-phase study with only 12 participants, so results may not apply to everyone. Ketamine can cause side effects like dizziness or dissociation, and its long-term effects in teens are not well known.
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 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
12 people
The number who actually took part.
- Started
-
Mar 2022
- Finished
-
Nov 2024
- Lead sponsor
-
A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
13 to 29 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. Major depressive episode including unipolar and bipolar depression, according to DSM- 5 criteria and MINI-adolescent version (Mini-International Neuropsychiatric Interview; MINI) diagnostic interview. 2. Age 13 to 19 years old. 3. Body weigh ≧ 30 kg. 4. Treatment-resistant depression, which is defined as poor or unsatisfactory response to at least two different antidepressants administered at an adequate dosage and for an adequate treatment duration 5. Still prominent depressive symptoms with at least 4-week treatment of medication treatment or psychotherapy 6. Voluntary patients and their parents or guardians with signed informed consent proved by institutional review board (IRB) Exclusion Criteria: 1. Major medical conditions (e.g., head injury, epilepsy, severe renal diseases and cancer). 2. Other axis I psychiatric disorders such as schizophrenia, delusional disorder, organic brain syndrome, and dementia. 3. Pregnancy. 4. Substance abuse in previous 6 months such as cocaine, marijuana, opium, ketamine, PCP (phencyclidine)。 5. Current use of NMDA receptor antagonist (Amantadine, Rimantadine, Lamotrigine, Memantine, Dextromethorphan) 6. Alcohol abuse / dependence within 6 months. 7. Attempt suicide in hospital. 8. Allergy to ketamine 9. Abnormal liver function in recent 3 months。 10. Abnormal ECG (i.e.:arrhythmia)。 11. Fever or infection in recent 5 days。
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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
-
Taipei Veterans General Hospital, Taiwan
Taipei, 112, Taiwan
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