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The NeuroStar TMS Device: Conducting the FDA Approved Protocol for Treatment of Depression
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November 12, 2010
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In this article, we examine the methodology and considerations relevant to the FDA approved depression treatment protocol using the Neuronetics NeuroStar TMS device.
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NeuroStar TMS DeviceFDA Approved ProtocolTreatment Of DepressionNeuroStar Transcranial Magnetic Stimulation (TMS) SystemClass II Medical DevicePulsed Magnetic FieldsElectrical CurrentsCortexPhysiological ChangesFunctional Brain ChangesO’Reardon Et Al.Industry-sponsored Clinical TrialMajor DepressionAntidepressant Treatment TrialActive TMSSham TMSLeft Dorsolateral Prefrontal Cortex (DLPFC)Medication-free PatientsMontgomery-Asberg Depression Scale (MADRS)Hamilton Depression Rating Scale (HAMD)FDA Approval
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Horvath, J. C., Mathews, J., Demitrack, M. A., Pascual-Leone, A. The NeuroStar TMS Device: Conducting the FDA Approved Protocol for Treatment of Depression. J. Vis. Exp. (45), e2345, doi:10.3791/2345 (2010).
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