This randomised, double-blind, placebo-controlled trial (n=26) aims to investigate the safety and efficacy of ketamine and riluzole in patients with treatment-resistant major depressive disorder. Additionally, the study will assess whether lamotrigine can mitigate ketamine-associated side effects.
Conducted by Baylor College of Medicine, the trial enrolled ketamine-responsive patients and randomly assigned them to either riluzole or placebo for a four-week continuation phase. The primary outcome was measured using the Montgomery-Åsberg Depression Rating Scale (MADRS) to evaluate depressive symptoms following ketamine infusion. Secondary outcomes included the effectiveness of lamotrigine in reducing ketamine’s psychotomimetic effects.
Trial Details
Trial Number
Sponsors & Collaborators
Baylor College of MedicineThis company doesn't have a full profile yet, it is linked to a clinical trial.
National Alliance for Research on Schizophrenia and Depression
This company doesn't have a full profile yet, it is linked to a clinical trial.
National Center for Research Resources
This company doesn't have a full profile yet, it is linked to a clinical trial.
Measures Used
Montgomery-Asberg Depression Rating ScaleA ten-item diagnostic questionnaire used to measure the severity of depressive symptoms in patients with mood disorders.