About this trial
The purpose of this study is to test the hypothesis that the anti-depressant and anti-suicidal effects of the N-methyl-D-aspartate receptor (NMDAR) antagonist Ketamine is critically dependent on stimulation of Alpha-Amino-3-Hydroxy-5-Methyl-4-Isoxazole Propionic Acid receptors (AMPAR).
Eligibility criteria
Qualifiers
Current depression as indicated by a score greater than 17 on the full Hamilton Depression Rating Scale (HDRS-17) AND current major depressive episode as determined by structured clinical interview (SCID-5)
Current suicidal ideation as indicated by a score ≥ 2 on the HDRS-17 Item #3 ("wishes to be dead (or any thoughts of possible death to self)")
Anti-depressant resistant depressive symptoms, defined by a history of failure of one or more adequate anti-depressant trials
Participants will meet DSM-5 Criteria for MDD, PTSD or Bipolar Disorder as determined by the SCID-5
Disqualifiers
A score on the Columbia-Suicide Severity Rating Scale [43] in the "intent" or "intent with plan" categories within the last 3 months or judged by Dr. Krystal or Dr. Driesen to be at serious risk for suicide.
Psychiatric hospitalization in the past two months
Suicide attempt in the past two months
More than half hour unconsciousness after trauma
Trial design
Treatments tested in this trial
- Perampanel 6 MG
- Ketamine
- Placebo
Treatment groups
Sponsors and collaborators
Yale University
Lead sponsor
American Foundation for Suicide Prevention
Collaborator
National Center for PTSD
Collaborator
VA Connecticut Healthcare System
Collaborator