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Clinical Trials/NCT03175887
NCT03175887
Withdrawn
N/A

Dorsolateral Versus Medial Prefrontal TMS for Depression

Overview

Phase
N/A
Intervention
Not specified
Conditions
Depression
Sponsor
White River Junction Veterans Affairs Medical Center
Locations
1
Primary Endpoint
Depressive symptoms measured by the 17-item Hamilton Depression Rating Scale
Status
Withdrawn
Last Updated
4 years ago

Overview

Brief Summary

This study is aimed to help us learn about the effects of Transcranial Magnetic Stimulation at the forehead versus the left side of the head for treatment of Treatment Resistant Depression.

Detailed Description

While transcranial magnetic stimulation (TMS) to the left dorsolateral prefrontal cortex (DLPFC) is an FDA approved treatment for depression, a growing and converging database suggests the medial prefrontal cortex (MPFC) may be even more critical to the neurobiology of depression and antidepressant treatment response. This study will compare the efficacy of high frequency transcranial madntic stimulation on these two sections of the brain.

Registry
clinicaltrials.gov
Start Date
September 2021
End Date
September 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Paul Holtzheimer

Director of Mood Disorder Services

White River Junction Veterans Affairs Medical Center

Eligibility Criteria

Inclusion Criteria

  • 21-70 years old
  • inadequate response to one current antidepressant medication
  • currently depressed

Exclusion Criteria

  • psychiatric comorbidities

Outcomes

Primary Outcomes

Depressive symptoms measured by the 17-item Hamilton Depression Rating Scale

Time Frame: Change from baseline Hamilton-17 score to follow-up visit at 1 week after final TMS intervention.

Depressive symptoms will be measured by the 17-item Hamilton Depression Rating Scale.

Study Sites (1)

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