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i-CBT and IV Ketamine for Suicidality in Treatment-Resistant Depression: A Randomized, Midazolam-Controlled Clinical Trial

Study acronym: Ket-CBT
StatusActive, Not Recruiting
PhasePhase 2
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 12 months later Mar 2026 → Mar 31, 2027
Enrollment reduced 31% 110 → 76 participants
See other at-risk trials from University Health Network, Toronto

Record History

  1. Notable Primary completion pushed from Mar 2026 to Mar 31, 2027 Enrollment reduced: 110 → 76 participants · Enrollment closed, study ongoing · Completion pushed from Jun 2026 to Mar 31, 2027 · 3 more Show 6 more changesShow less
    • Enrollment reduced: 110 → 76 participants
    • Enrollment closed, study ongoing
    • Completion pushed from Jun 2026 to Mar 31, 2027
    • Eligibility criteria expanded, about 18 words
    • Secondary endpoints: details revised at 22 of 32 entries
    • Site details revised
  2. Minor Study sites: 2 to 1v3
  3. Notable Primary completion date: Apr 2025 to Mar 2026 Completion date: Jul 2025 to Jun 2026v2 Show 1 more changeShow less
    • Completion date: Jul 2025 to Jun 2026
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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 76 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.
Trial Details
NCT Number NCT06480500
Lead Sponsor University Health Network, Toronto
Collaborators: Ontario Shores Centre for Mental Health Sciences
Conditions Major Depressive Disorder, Suicide, Treatment Resistant Depression
Enrollment 76 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov