drugset / Trial / NCT03237286

Intravenous Ketamine Plus Neurocognitive Training for Depression

NCT03237286

RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study has two aims: 1) to characterize the effects of intravenous ketamine on neurocognitive markers in depressed patients; 2) to test the efficacy of a synergistic intervention for depression combining intravenous ketamine with neurocognitive training. Three of the primary outcomes listed (fMRI functional connectivity; Implicit Association Test; cognitive flexibility testing) pertain to Aim 1. For Aim 2, one primary clinical outcome (MADRS, a clinician-administered measure of depression severity) pertains to the acute (30-day) phase, while the QIDS (a self-report measure of depression severity) becomes the primary clinical outcome during the 12-month naturalistic follow-up.

Timeline

Start
2017-12-01
Primary completion
2022-10-18
Completion
2022-10-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Ketamine Small molecule Intravenous

Indications