Actively Recruiting
i-CBT and IV Ketamine for Suicidality in Treatment-Resistant Depression: A Randomized, Midazolam-Controlled Clinical Trial
Led by University Health Network, Toronto · Updated on 2025-12-05
110
Participants Needed
1
Research Sites
125 weeks
Total Duration
On this page
Sponsors
U
University Health Network, Toronto
Lead Sponsor
O
Ontario Shores Centre for Mental Health Sciences
Collaborating Sponsor
AI-Summary
What this Trial Is About
Approximately four thousand Canadians die by suicide every year, and suicide is the second leading cause of death in youth and young adults (15-34 years). Most people with depression experience thoughts of suicide and many will also plan and/or attempt suicide at some time in their life. There is an urgent need for new scalable treatments that can effectively reduce suicidality in people with depression. Cognitive behavioural therapy (CBT) reduces suicidal thoughts and behaviours, and can be delivered through the internet (i-CBT) making it more accessible and scalable. However, i-CBT has not been shown to rapidly reduce suicidal thoughts and behaviours (suicidality), such as within 24 hours. IV ketamine on the other hand has been shown to rapidly reduce thoughts of suicide, but not suicidal behaviours. Therefore, combining i-CBT with IV ketamine may be more effective reducing suicidality than i-CBT treatment with a control treatment. The investigators propose a 13-week, multi-site, study that looks at how combining i-CBT and IV ketamine treatment will affect suicidality in individuals with depression who have recently experienced suicidal thoughts and/or behaviours, but have not responded to previous treatment. All 110 participants will receive a weekly session of i-CBT for 13 weeks, but half will be randomly assigned to also receive six IV ketamine treatments or six IV midazolam treatments (control treatment) over the first initial 30 days. The investigators will measure changes in suicidal thoughts and behaviours before drug treatment and at the primary endpoint (i.e.,day 30), and after 3 months (i.e. Day 91) of the starting treatment.
CONDITIONS
Official Title
i-CBT and IV Ketamine for Suicidality in Treatment-Resistant Depression: A Randomized, Midazolam-Controlled Clinical Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Provide written, voluntary informed consent before joining the study.
- Be male or female aged 21 to 65 years.
- Have a diagnosis of Major Depressive Disorder with a current Major Depressive Episode without psychotic features, confirmed by a structured interview.
- Have moderate to severe depression with a MADRS score above 21.
- Be at risk for suicide based on responses to the Columbia-Suicide Severity Rating Scale.
- Have had an inadequate response to two or more adequate first-line treatments for depression.
- Have reliable internet access and an internet-enabled device for the entire study.
- Be able to read and speak English, as therapy is offered only in English.
You will not qualify if you...
- Currently have symptoms of mania, hypomania, or mixed bipolar state with a Young Mania Rating Scale score above 12.
- Have current symptoms of psychosis or substance use disorder within the past 3 months.
- Have a lifetime history of a primary psychotic disorder such as schizophrenia.
- Have a lifetime history of ketamine use disorder.
- Have neurological disorders like uncontrolled seizures, recent stroke, major head injury, or vascular diseases.
- Have contraindications to ketamine or midazolam including allergies, uncontrolled hypertension, recent heart attack, arrhythmia, severe heart or liver disease, or severe kidney impairment.
- Are pregnant, breastfeeding, or planning to become pregnant and unwilling to use effective contraception.
- Use prohibited medications like other forms of ketamine, benzodiazepines, monoamine oxidase inhibitors, stimulants, or medical cannabis.
- Are currently receiving cognitive behavioural therapy or related therapy.
- Have changed medication or psychotherapy within one month before joining the study.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Toronto General Hospital
Toronto, Ontario, Canada
Actively Recruiting
Research Team
S
Simryn Selby, MSc
CONTACT
O
Orly Lipsitz
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here