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Open-label Prospective, Interventional Study Assessing Efficacy and Safety of Intramuscular Ketamine for Suicidal Ideation in a Tertiary Care Hospital.

Malika M Sanspara, Drashti M Shah, Sandip H Shah, Nimisha D Desai, Saurabh N Shah, Preet Patel

Indian journal of psychological medicine November 13, 2025 DOI: 10.1177/02537176251389117 via PubMed

Summary

AI-generated from the abstract

A single intramuscular injection of ketamine (0.5 mg/kg) rapidly reduces suicidal ideation in adults, with a 78% decrease in MADRS-SI scores within two hours and 76% of patients reporting no suicidal ideation. Among 38 patients, 89% of those completing one-month follow-up maintained the reduction. Most patients required only one injection, though 36% needed multiple doses. Common side effects were dizziness and sedation, but no serious adverse events occurred. The study suggests IM ketamine is a safe and effective fast-acting option for suicidal ideation in settings where intravenous treatment is impractical.

Study at a glance

Characteristics Pre-post-interventional study Open-label Peer reviewed
Sample size 38
Population Adult patients with suicidal ideation (MADRS-SI score >4)
Intervention Intramuscular ketamine
Dose 0.5 mg/kg
Duration 28-day follow-up (with additional follow-up at six months for some patients)
Keywords Intramuscular ketamine Madrs-si Rapid intervention Treatment Approach
Key finding Intramuscular ketamine (0.5 mg/kg) produced a rapid and sustained reduction in suicidal ideation, with a 78% mean score reduction at two hours and no serious adverse effects.

Abstract

This study evaluated intramuscular (IM) ketamine's efficacy and safety for rapid suicidal ideation reduction, addressing the critical need for fast-acting interventions in resource-limited settings where intravenous (IV) options are impractical. We conducted a pre-post-interventional study of IM ketamine (0.5 mg/kg) over one year after approval of the institutional ethics committee. Adult patients with suicidal ideation, as measured by the six-point Montgomery-Åsberg Depression Rating Scale-Suicidal Ideation (MADRS-SI), were included if their MADRS-SI score was >4. Post-injection monitoring of suicidal ideation and adverse effects (A/E) was done after two hours and on Days 1, 3, 7, 14, 21, and 28. A repeat injection of the same dose was given only if the MADRS-SI score became > 4 again. The paired-T-test and repeated-measure ANOVA test were used for statistical analysis. Thirty-eight patients (mean age: 36.3 years) participated, with 66% diagnosed with major depressive disorder and a mean MADRS-SI score of 5.31. At two hours post-injection, the MADRS-SI score decreased by 4.13 points (78% reduction), with 76% (N = 29) of patients reporting no suicidal ideation (score 0-1). Of the 28 patients who completed a one-month follow-up, 89% (N = 25) maintained a reduction in suicidal ideation (mean reduction: 4.75 points). A total of 64% (N = 16) required only one injection, while 36% required multiple injections. Three patients did not recover even after six trials of ketamine. Among 21 patients who completed six months of follow-up, 8 (28%) patients had relapsed. A/E was reported in 87% of patients, with dizziness and sedation being the most common (57%). No serious or life-threatening adverse effects were noted. IM ketamine (0.5 mg/kg) is effective and safe for the rapid reduction of suicidal ideation.

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