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The NeuroStar TMS Device: Conducting the FDA Approved Protocol for Treatment of Depression
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JoVE Journal Neuroscienze
The NeuroStar TMS Device: Conducting the FDA Approved Protocol for Treatment of Depression

The NeuroStar TMS Device: Conducting the FDA Approved Protocol for Treatment of Depression

DOI:
10.3791/2345-v

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10:29 min

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November 12, 2010

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, , ,
1Berenson-Allen Center for Noninvasive Brain Stimulation,Beth Israel Deaconess Medical Center, 2Neuronetics,Inc.

Capitoli

  • 00:00Titolo
  • 01:19Preparation
  • 02:24Seating and Aligning the Patient
  • 04:27Determine Motor Threshold
  • 07:46Patient Treatment
  • 09:50Results of Treatment with the NeuroStar System
  • 10:07Conclusion

Summary

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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.

Tags

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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