This study is currently not recruiting participants.

A Prospective, Multicenter, Double-Blind, Sham-Controlled Study to Confirm the Safety and Efficacy of s-TMS in Treatment of Major Depressive Disorder

  • STATUS
    Not Recruiting
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Updated on 19 February 2024

Summary

This study is a multicenter, randomized, double-blind, sham-controlled trial to confirm the safety and efficacy of NEST sTMS device in treatment of subjects with major depressive disorder who have not responded to at least one antidepressant treatment.

Description

Patients who decide to participate in this study will be randomized to either receive the active or simulated (sham) treatment. Synchronized transcranial magnetic stimulation (sTMS) is a non-invasive method for stimulating cells in your brain using magnetic fields generated by magnetic coils placed near your head. The study duration is 6 weeks for 5 daily study treatment sessions per week, for a total of 30 study treatments. Following completion of all study treatments, you may be eligible for an additional 6 weeks of treatment with active sTMS therapy. The study treatment and all tests, procedures and visits required by the study are provided at no cost to you.

FAQ

You might be eligible to participate in this study if you have been diagnosed with Major Depressive Disorder and have tried at least one antidepressant but haven’t experienced at least 50 % improvement in your symptoms. The study doctor will discuss additional requirements for being in the study with you.

Details
Condition Mitral Valve Insufficiency,,mitral valve insufficiency
Age 18years - 70years
Clinical Study IdentifierTX5885
Last Modified on19 February 2024

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