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The UTHealth Ketamine Project
TerminatedRegisteredCTG
The primary objective of this study is to determine the effectiveness of serial infusions of intravenous (IV) ketamine in adults with treatment-resistant depression (TRD).
Details
Open-label, single-group treatment study of 10 adults with treatment-resistant depression receiving serial slow IV ketamine infusions (0.5 mg/kg over 40 minutes).
Dosing schedule: twice weekly for 4 weeks then weekly for 4 weeks (12 total infusions). Primary outcome is remission based on depressive severity; a four-week observational follow-up will record clinical status and include a neurocognitive task.
Topics:Treatment-Resistant Depression (TRD)
Registry
Registry linkNCT02882711