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Clinical Trial Summary

This study evaluates an accelerated schedule of theta-burst stimulation for inpatients with major depressive disorder

Clinical Trial Description

This study intends to investigate whether modifying stimulation parameters enables typical 6-8 week long rTMS protocols to be compressed to only five days. The influence of this accelerated protocol on the length of patient stay in the hospital and the direct total cost will be investigated. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT03693105
Study type Interventional
Source Stanford University
Contact Eleanor Cole, PhD
Phone 415-724-7960
Status Not yet recruiting
Phase N/A
Start date February 2019
Completion date June 2020

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