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Ketamine for Acute Suicidal Ideation in the Emergency Department: Randomized Controlled Trial

NCT01892995 · LDK-SI · Brooke Army Medical Center

Closed to entry
Status
Not accepting participants
Not applicable
Phase
53
Target enrolment
1
Study sites
1 US states

What it is testing

Summary

This study will enroll patients presenting to the emergency department with acute suicidal ideation meeting inclusion and exclusion criteria. Patients will be randomized to one of three arms: ketamine (intervention) or diphenhydramine (control) or placebo (control). Serial measurements will be made in the ED and at follow-up intervals.

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • Change in Beck Scale for Suicidal Ideation

    Measured over 2 hours

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

18 Years to 75 Years
Ages
All
Sex
Accepted
Healthy volunteers
Inclusion Criteria: * Patients age 18 to less than 75 who present to the SAMMC ED with either overt or incidental suicidal ideations with a SADPERSONS score 5 or greater that the treating provider feels warrant formal evaluation. Exclusion Criteria: * -Poor vital sign stability hypoxia: O2 \< 95%, hypotension: SBP\< 90 hypertension: SBP\>180 Heart rate: \< 50 or \>120 Respiratory Rate: \<10 or \>30 * Altered mental status or intoxication * Patient is unwilling to participate or provide informed consent * Any allergy to ketamine or diphenhydramine * Patient is female of child-bearing age and unwilling to provide urine or blood for HCG analysis * Pregnancy or breast feeding * Presence of chronic oxygen-dependent pulmonary disease, liver cirrhosis, or renal disease requiring dialysis * Presence of ischemic heart disease, heart failure, or a history of unstable dysrhythmias * Presence of intracranial mass or vascular lesion. * Presence of a history of psychosis or hallucinations (as assessed by electronic chart review) * Weight greater than 115 kg or less than 45kg * History of increased intracranial pressure/hypertensive hydrocephalus * Non-English speaking patients * Patient is acutely psychotic * Provider feels that patient currently or likely will require chemical and/or physical restraints * History of prolonged QT-interval

Where

1 study site

FacilityCityRegionCountry
Brooke Army Medical CenterFort Sam HoustonTexasUnited States

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT01892995 on ClinicalTrials.gov →

Last updated in the registry 2015-02-16. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits