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Clinical Trial Summary

The goal of this observational study is to demonstrate effectiveness in the treatment of Major Depressive Disorder The primary objective is to assess the effectiveness in the treatment of Major Depressive Disorder using the CGI-I at the end of the treatment Participants will receive 10 treatments per day for 5 days (M-F) of SAINT®


Clinical Trial Description

This is a prospective, multi-center, open-label study. Up to 1000 adult subjects, in a major depressive episode, who have failed to receive satisfactory improvement from a prior antidepressant medication in the current episode, are eligible to participate in this study if they are deemed to be appropriate candidates for TMS. Overall study duration is expected to be approximately 4 years. The study duration per subject is anticipated to be approximately 1 year. Hypothesis: The SAINT® Neuromodulation System will demonstrate effectiveness in the treatment of MDD as measured by CGI-I at the end of the treatment (cessation of stimulation). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05819021
Study type Observational
Source Magnus Medical
Contact Jessica Hawkins
Phone 650-525-4485
Email jessica@magnusmed.com/https://www.magnusmed.com/clinical-trials/
Status Recruiting
Phase
Start date April 6, 2023
Completion date April 15, 2027

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