Sustained Ketamine Effectiveness for Suicidal Ideation (SKESI)

This observational cohort study (n=128) will evaluate the sustained effectiveness of intravenous (IV) ketamine for suicidal ideation in adults experiencing a suicidal crisis due to major depressive disorder.

Conducted at the University Hospital, Montpellier, this retrospective study analyses medical records of patients treated with IV ketamine in the Psychiatric Emergency and Post-Emergency Department between June 2022 and March 2024.

The study aims to assess changes in suicidal ideation and behaviour at multiple time points—7 days, 1 month, and 3 months post-treatment—using the Columbia-Suicide Severity Rating Scale (C-SSRS). Secondary outcomes include evaluating depressive symptoms through the Montgomery-Åsberg Depression Rating Scale (MADRS) and tracking hospitalisations or emergency visits related to suicidal ideation.

Trial Details



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