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Neurobiology of Suicide

StatusRecruiting
PhasePhase 2
Started
View on ClinicalTrials.gov ↗

Record History

The 50 most recent of 297 record versions are accounted for below. See every version on ClinicalTrials.gov ↗

  1. Minor Eligibility criteria expanded, about 57 words
    • Secondary endpoints revised (2)
    • Publications: 5 to 6
  2. Minor 18 versions Re-verified since Mar 26, 2026, no change to tracked fieldsv279-v296
  3. Notable Primary and study completion dates: Jul 21, 2026 to Jul 21, 2030v278
  4. Minor 8 versions Re-verified since Aug 26, 2025, no change to tracked fieldsv270-v277
  5. Notable Primary and study completion dates: Jul 21, 2025 to Jul 21, 2026v269
Show 21 earlier versionsHide 21 earlier versions
  1. Minor Eligibility criteria shortened, about 1 word
    • Study description shortened, about 2 words
    v268
  2. Minor 20 versions Re-verified since Mar 6, 2025, no change to tracked fieldsv248-v267
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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. ...
Trial Details
NCT Number NCT02543983
Lead Sponsor National Institute of Mental Health (NIMH)
Conditions
(from sponsor)
Healthy Volunteers, Depression
Related terms Depression, Major Depressive Disorder, Suicide
Enrollment 325 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov