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

30 Participants
are divided into 2 treatment groups

Locations

1
VA Connecticut Healthcare System06516, West HavenConnecticut, United States

Sponsors and collaborators

Yale University

Lead sponsor

American Foundation for Suicide Prevention

Collaborator

National Center for PTSD

Collaborator

VA Connecticut Healthcare System

Collaborator