NCT05045378CompletedPhase 4
Low-dose Ketamine Infusion Among Adolescents With Treatment-resistant Depression
Low-dose Ketamine Infusion Among Adolescents With Treatment-resistant Depression: a Randomized, Double-blind Placebo-control Study
Source: ClinicalTrials.gov · Last updated 5 Sept 2025
Brief summary (registry, in English)
In the past decades, the prevalence of adolescent depression and suicide increased significantly in Taiwan and worldwide. To date, the suicide mortality is the second mortality cause in the adolescent and young adult population in Taiwan. Previous studies reported that up to 40% of adolescents with major depressive disorder did not respond to at least two traditional antidepressants with the optimal dose and adequate duration. Those patients would be considered the cases with treatment-resistant depression (TRD), which is related to the poor prognosis, chronic depressive course, higher suicidal risk, severer cognitive dysfunction, and greater family burdens. However, much less studies investigated the treatment strategy for adolescent TRD compared with that for adult TRD. In this decade, low-dose ketamine infusion has been proved as a rapid-acting antidepressant for adult patients with TRD. In recent 5 years, the investigators study team finished two randomized, double-blind, and placebo-control trials to support the rapid antidepressant and anti-suicidal effect in Taiwanese adult patients with TRD. The investigators published several SCI studies about the investigators clinical findings and the underlying brain mechanisms. In the following 4 years, the investigators will conduct a new randomized, double-blind, and placebo-control trial in the adolescent TRD. It will be the first clinical trial for ketamine effect in adolescent TRD worldwide. The investigators will enroll 54 adolescents aged between 13 and 29 with TRD in four years. The investigators hypothesize that low-dose ketamine will be effective and well tolerable for adolescents with TRD.
- Status (registry)
- Completed
- Phase (registry)
- Phase 4
- Study type
- Interventional
- Enrollment
- 12 (actual)
- First submitted
- 7 Sept 2021
- Start date
- 15 Mar 2022
- Primary completion date
- 30 Nov 2024
- Lead sponsor
- Taipei Veterans General Hospital, Taiwan
- Diseases
- Depression
- NCT number
- NCT05045378
What you commit to
- Study type: Interventional · Phase 4
- Participants enrolled: 12
- From 15 Mar 2022 to the primary completion date, 30 Nov 2024
- 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
- Substance abuse in previous 6 months such as cocaine, marijuana, opium, ketamine, PCP (phencyclidine)。
Other illness
- Major medical conditions (e.g., head injury, epilepsy, severe renal diseases and cancer).
- Other axis I psychiatric disorders such as schizophrenia, delusional disorder, organic brain syndrome, and dementia.
- Allergy to ketamine
- Abnormal ECG (i.e.:arrhythmia)。
- Fever or infection in recent 5 days。
Other
- Pregnancy.
- Current use of NMDA receptor antagonist (Amantadine, Rimantadine, Lamotrigine, Memantine, Dextromethorphan)
- Alcohol abuse / dependence within 6 months.
- Attempt suicide in hospital.
- Abnormal liver function in recent 3 months。
Who the study is looking for
- Major depressive episode including unipolar and bipolar depression, according to DSM- 5 criteria and MINI-adolescent version (Mini-International Neuropsychiatric Interview; MINI) diagnostic interview.
- Age 13 to 19 years old.
- Body weigh ≧ 30 kg.
- 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
- Still prominent depressive symptoms with at least 4-week treatment of medication treatment or psychotherapy
- Voluntary patients and their parents or guardians with signed informed consent proved by institutional review board (IRB)
Age in the registry: 13 years to 29 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Taipei Veterans General Hospital, Taiwan Coordinator of this site? Confirm its status | Taipei | Taiwan | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.