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RecruitingSuicideSuicidal IdeationDepression

Feasibility and Safety of Ketamine for Suicidal Patients in the Emergency Department

Eligible age

18–65 yrs

Accepts

All genders

Locations

1 state

Healthy volunteers

No

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About this study

There is currently no readily available pharmacologic intervention for suicidal ideation, a true psychiatric emergency, in the Emergency Department (ED). Investigators aim to trial low-dose, intravenous ketamine, a drug with well-established use in treatment-resistant depression, for patients who present to the ED with suicidal ideation.

Sponsor: Lindsay Maguire, MD

You may qualify if…

  • Acutely Suicidality ("yes" answer to any of items 4 or 5 on C-SSRS "Suicidal Ideation" category)
  • Require inpatient stabilization for SI or actions based on clinical observation and interview
  • Are accepted for psychiatric stabilization at the University of Kansas Medical Center's Strawberry Hill campus
  • Have a Glasgow Coma Score (GCS) of 15
  • Age 18-65

You may not qualify if…

  • Current or past history of psychosis
  • Current or recent (past 4 weeks) symptoms of mania/hypomania as defined by Young Mania Rating Scale (YRMS) score of 12 or greater
  • History of ketamine use disorder
  • History of liver transplant
  • Pregnancy or breastfeeding
  • Imprisonment or inability to consent
  • Positive urine drug screen or serum alcohol level
  • Hypertension (SBP \> 160 or DBP \> 100 before administration of ketamine)

Where it's recruiting

Kansas

Kansas City

Source: ClinicalTrials.gov · NCT06085937 · last updated 2026-04-15

Feasibility and Safety of Ketamine for Suicidal Patients in the Emerge · TrialPath