CompletedN/Aketamine
Ketamine Infusion for Treatment-resistant Major Depressive Disorder
Sponsored by Massachusetts General Hospital
NCT ID
NCT01582945
Target Enrollment
14 participants
Start Date
2012-04
Est. Completion
2014-12
About This Study
Ketamine infusion has been shown to have rapid antidepressant properties, however the possible use of ketamine in treatment-resistant depression as augmentation has not been investigated. The overall aim of this study is to assess the feasibility, safety and tolerability, efficacy and duration of the effect of intravenous N-methyl-D-aspartate antagonist ketamine as augmentation of antidepressants for chronic suicidal ideation in subjects with severe treatment-resistant depression (TRD). This is an open-label study (pilot).
Conditions Studied
Interventions
- •Ketamine
Eligibility
Age:18 Years - 65 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria: * Outpatients with severe treatment-resistant MDD * Currently depressed * Currently under regular psychiatric care * On an aggressive antidepressant regimen, stable for 4 weeks Exclusion Criteria: * No history of other major psychiatric illnesses, including bipolar disorder * No history of psychosis * No history of drug abuse * No major medical illness or unstable medical conditions
Study Locations (1)
Depression Clinical and Research Program - MGH
Boston, Massachusetts, United States