Personalized rTMS for Resistant Depression

Status Terminated

Clinical Trial Summary

The investigators hypothesize that personalizing the rTMS targets using functional MRI will increase its efficacy. The most dysfunctional regions or the most dysfunctional network will be stimulated homogeneously. Individualized rTMS will be compared to traditional rTMS procedure and to trans-cranial direct current stimulation (tDCS) in a randomized cross-over trial. In this pilot study the primary outcome measure will be the correction of the MRI anomalies. Symptoms reduction and the proportion of remitters will be secondary outcome measurements.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02863380
Study type	Interventional
Source	University Hospital, Strasbourg, France
Contact
Status	Terminated
Phase	N/A
Start date	May 4, 2016
Completion date	January 21, 2021

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