Actively Recruiting
Neurobiology of Suicide
Led by National Institute of Mental Health (NIMH) · Updated on 2026-03-27
325
Participants Needed
1
Research Sites
763 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Background: There are no good treatments for people considering suicide. Researchers want to study suicide with questions, blood tests, brain imaging, and sleep studies. They hope to better understand suicide, so they can help suicidal people. Objective: To understand what happens in the brain when someone has thought about or attempted suicide. Eligibility: Group 1: Adults ages 18 70 who have thought about or attempted suicide recently Group 2: Adults ages 18 70 who have thought about or attempted suicide in the past Group 3: Adults ages 18 70 who have depression or anxiety, but have never thought about suicide Group 4: Healthy volunteers the same ages. Design: Participants will be screened in another protocol. Adults who have recently thought about or attempted suicide must be referred by a doctor. They may do up to 3 phases of this study. Groups 2, 3 and 4 will do only Phase 1 and will not get ketamine. Phase 1: 1 week in hospital. Participants will have: Physical exam. Questions about thoughts and feelings. Thinking and memory tests and simple tasks. Blood and urine tests. Two MRI scans. Participants will lie on a table that slides into a metal cylinder that takes pictures. They will have a coil over their head and earplugs and do a computer task. Sleep test. Disks and bands will be placed on the body to monitor it during sleep. Magnetic detectors on their head while they perform tasks. A wrist monitor for activity and sleep. Lumbar puncture (optional). A needle will collect fluid from the back. Shock experiments (optional). Participants will observe pictures and sounds and feel a small shock on the hand. Phase 2: 4 days in hospital. A thin plastic tube will be placed in each arm, one for blood draws, the other to get the drug ketamine once. Participants will repeat most of the Phase 1 tests. Phase 3: up to 4 more ketamine doses over 2 weeks. Participants will have follow-up calls or visits at 6 months and then maybe yearly for 5 years.
CONDITIONS
Official Title
Neurobiology of Suicide
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 to 70 years
- Ability to understand and consent to tests and examinations
- Individuals able to get pregnant must use effective birth control or remain sexually abstinent during study phases
- Group 1 participants must agree to be hospitalized
- For Phase II, participants must have completed Phase I as Group 1 or 5 and show minimal suicidal, depressive, or anxiety symptoms
- For Phase III, participants must have completed Phase II as Group 1 or 5
You will not qualify if you...
- Current psychotic features or cognitive impairment preventing study understanding
- Current drug or alcohol dependence or acute intoxication
- Pregnant, nursing, or planning pregnancy
- Serious unstable medical conditions including liver, kidney, heart, lung, endocrine, neurological, immune, or blood diseases
- Abnormal lab tests or positive HIV test
- Individuals posing unmanaged suicide or homicidal risk
- Non-English speakers
- Group 4 exclusions: psychiatric history, substance abuse, suicide history, medical illnesses affecting brain
- MRI exclusions: implanted metal devices, claustrophobia, brain abnormalities, diagnosed hearing loss
- Phase II and III exclusions: use of reversible MAOIs recently, certain medications, seizure history, positive drug tests, psychotic disorders, adverse reactions to ketamine
AI-Screening
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Trial Site Locations
Total: 1 location
1
National Institutes of Health Clinical Center
Bethesda, Maryland, United States, 20892
Actively Recruiting
Research Team
L
Laura R Waldman, L.C.S.W.
CONTACT
C
Carlos A Zarate, M.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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