10
Participants
Start Date
October 1, 2025
Primary Completion Date
March 15, 2026
Study Completion Date
April 15, 2026
Ketamine only
The primary study intervention involves the administration of intravenous ketamine (0.5 mg/kg) over a 40-minute infusion. Ketamine, an NMDA receptor antagonist, has shown rapid antidepressant effects in individuals with treatment-resistant depression.
University of Pennsylvania
OTHER