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Investigational TMS Treatment for Depression

Dorsolateral Versus Medial Prefrontal TMS for Depression

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03175887
Enrollment
0
Registered
2017-06-05
Start date
2021-09-30
Completion date
2022-09-30
Last updated
2021-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression, Treatment Resistant Depression

Keywords

depression, trd, treatment-resistant depression, TMS

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.

Interventions

DEVICETMS

Transcranial magnetic stimulation (TMS) is a noninvasive procedure that uses magnetic fields to stimulate nerve cells in the brain to improve symptoms of depression.

Sponsors

White River Junction Veterans Affairs Medical Center
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
21 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

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

Exclusion criteria

* psychiatric comorbidities

Design outcomes

Primary

MeasureTime frameDescription
Depressive symptoms measured by the 17-item Hamilton Depression Rating ScaleChange 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.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026