CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 33 enrolled
Drug / intervention
transcranial magnetic stimulationdevice
Likely dose
Not stated in record
Key inclusion· 7
  • Age 18-60 years, male or female outpatients
  • Confirmed Major Depressive Disorder diagnosis via SCID-IV-TR
  • Current depressive episode ≥1 month duration
  • HDRS-17 score ≥18 despite adequate trial of serotonin reuptake inhibitor
Key exclusion· 10
  • Lifetime history of Bipolar Disorder or any Psychotic Disorder
  • Substance abuse or dependence in past year (except nicotine/caffeine)
  • Significant neurological disorders: tics, brain lesions, seizure history (except therapeutic ECT), cerebrovascular accident, fainting, TIA within 2 years, aneurysm, dementia, Parkinson's, Huntington's, MS
  • Increased seizure risk including history of elevated intracranial pressure or significant head trauma with ≥5 minutes loss of consciousness

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02974296
NCT02974296N/ACompleted

Neuroimaging in Patients Undergoing TMS for Depression

New York State Psychiatric Institute·interventional·Posted Nov 28, 2016·Updated Oct 23, 2020

In Brief

A clinical study evaluating transcranial magnetic stimulation for Treatment Resistant Depression. Completed, enrolled 33 participants across 1 site.

Detailed Summary

The goal of this project is to guide rTMS using functional magnetic resonance imaging (fMRI) in individuals with depression who did not respond to standard TMS treatment to evaluate whether targeted TMS using individualized functional MRI scans produce outcome superior to that of conventional approaches. The study team also plans to scan patients with Major Depression Disorder (MDD) patients prescribed to receive standard TMS for the first time before and after which they will have resting-state Functional Magnetic Resonance Imaging (rs-FMRI) scan in order to see if we can predict their responsiveness based on the functional connectivity maps.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedNov 28, 2016
Enrollment StartApr 30, 2017
Primary CompletionAug 20, 2019
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 9.6 years ago

Interventions

transcranial magnetic stimulationdevice

non invasive brain stimulation approach