18
Participants
Start Date
January 3, 2019
Primary Completion Date
December 31, 2026
Study Completion Date
December 31, 2026
Ketamine
We will enroll 20 adults (aged 18-65 years) with treatment-resistant depression and will provide two i.v. ketamine infusions (0.5 mg/kg, infused over 40 minutes) and measure their depressive symptom responses. Biomarkers will be developed using blood samples from study subjects, taken prior to (predictive biomarkers), and following ketamine treatment (change biomarkers). This will be an open-label feasibility trial.
Mayo Clinic in Rochester, Rochester
Lead Sponsor
Mayo Clinic
OTHER