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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