Ketamine & Crisis Response Plan for Suicidal Ideation in the ED

Recruiting Phase 2 Phase 3 Interventional Study
Suicide
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 70
Sex
Any
Trial phase
Phase 2/3
Study type
Interventional
Purpose
Other
Participants needed
24 (estimated)
Sponsor
The University of Texas Health Science Center at San Antonio · Other
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About This Trial
The goal of this randomized pilot trial is to assess the feasibility of administering a combination of 100mg intramuscular (IM) ketamine and Crisis Response Plan (a short psychosocial intervention) for patients with acute suicidality in the context of the Emergency Department setting. This study will assess a combination of a pharmacologic intervention and a psychosocial one. The pharmacologic int…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Adult men and women between the ages of 18 and 70 presenting to the Emergency Department with acute suicidal ideation. * Patient cleared for admission to the University Hospital inpatient psychiatric unit. * Decision to admit the patient to the inpatient unit or psychiatric st…
Contacts

Stehanie Perez, MHA

2104508973

perezs11@uthscsa.edu

CONTACT