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NMDA receptor antagonist

IM Ketamine vs Midazolam for Suicidal Thoughts

Phase 4
Waitlist Available
Led By Michael Grunebaum, MD
Research Sponsored by New York State Psychiatric Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
DSM5 unipolar or bipolar (I, II, or Unspecified) major depressive episode
Presenting to emergency department and assessed by psychiatrist staff as needing inpatient treatment due to suicidality
Must not have
Medical contraindication to ketamine or midazolam
Inadequate understanding of English and/or lack of capacity for informed consent
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 hours post-treatment
Awards & highlights

Summary

This trial tests whether a shot of ketamine can quickly reduce suicidal thoughts in depressed adults who visit the emergency room. These patients are at high risk of suicide and need fast-acting treatment. Ketamine works by quickly changing brain chemicals to improve mood and reduce suicidal thoughts. It has been found to rapidly reduce depressive symptoms and suicidal thoughts, making it a potential fast-acting treatment for suicidality.

Who is the study for?
This trial is for adults in the emergency department with severe depression and suicidal thoughts who need hospitalization. They must have a certain score indicating suicidality, be experiencing a major depressive episode, and agree to stay in the hospital. It's not for pregnant women, those unable to consent or understand English, people with unstable health conditions like uncontrolled high blood pressure or heart issues, recent substance abuse, psychosis or mania, or intellectual disability.
What is being tested?
The study tests if an injection of ketamine can quickly reduce suicidal thoughts in patients compared to midazolam (a sedative). Participants are given one of these drugs while they're in the emergency room being evaluated for serious mental health concerns.
What are the potential side effects?
Ketamine may cause disorientation, elevated blood pressure, nausea or mood changes shortly after administration. Midazolam can lead to drowsiness, reduced breathing rate and coordination difficulties. Both drugs carry risks that vary based on individual health status.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I have been diagnosed with a major depressive episode.
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I was advised to get inpatient treatment for suicidal thoughts by a psychiatrist.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I cannot take ketamine or midazolam due to health reasons.
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I understand English well and can make informed decisions about my health.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 hours post-treatment
This trial's timeline: 3 weeks for screening, Varies for treatment, and 24 hours post-treatment for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Scale for Suicidal Ideation (SSI)
Secondary study objectives
Systematic Assessment for Treatment Emergent Events (SAFTEE)

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: KetamineExperimental Treatment1 Intervention
Ketamine hydrochloride 0.5 mg/kg IM single injection
Group II: midazolamActive Control1 Intervention
Midazolam 0.06 mg/kg IM single injection

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Intramuscular ketamine is being studied for its rapid relief of suicidal thoughts due to its unique mechanism of action. Ketamine works primarily as an NMDA receptor antagonist, which leads to an increase in glutamate levels and subsequent activation of AMPA receptors. This cascade results in enhanced synaptic plasticity and connectivity, which can rapidly improve mood and reduce suicidal ideation. This rapid action is crucial for suicidal patients who require immediate intervention to prevent self-harm. Other treatments, such as SSRIs and SNRIs, work by increasing serotonin and norepinephrine levels but typically take weeks to show effects, making them less suitable for acute suicidal crises.

Find a Location

Who is running the clinical trial?

New York State Psychiatric InstituteLead Sponsor
477 Previous Clinical Trials
153,938 Total Patients Enrolled
National Institute of Mental Health (NIMH)NIH
2,869 Previous Clinical Trials
2,777,446 Total Patients Enrolled
1 Trials studying Suicidal Thoughts
240 Patients Enrolled for Suicidal Thoughts
Michael Grunebaum, MD4.36 ReviewsPrincipal Investigator - New York State Psychiatric Institute/Columbia University Irving Medical Center
New York State Psychiatric Institute
1 Previous Clinical Trials
8 Total Patients Enrolled
5Patient Review
I've been blown away by how well Dr. Grunebaum has been able to treat me remotely during the pandemic. I would have thought that telehealth would be a poorer substitute for in-person visits, but I've been pleasantly surprised.

Media Library

Ketamine hydrochloride injection (NMDA receptor antagonist) Clinical Trial Eligibility Overview. Trial Name: NCT04640636 — Phase 4
Suicidal Thoughts Research Study Groups: Ketamine, midazolam
Suicidal Thoughts Clinical Trial 2023: Ketamine hydrochloride injection Highlights & Side Effects. Trial Name: NCT04640636 — Phase 4
Ketamine hydrochloride injection (NMDA receptor antagonist) 2023 Treatment Timeline for Medical Study. Trial Name: NCT04640636 — Phase 4
~22 spots leftby Dec 2025