CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 12 enrolled
Drug / intervention
Active Neuronetics rTMS stimulator +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

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

Search/NCT02080507
NCT02080507N/ACompleted

rTMS in Treatment Resistant Depression

Emory University·interventional·Posted Mar 6, 2014·Updated May 30, 2017

In Brief

A clinical study evaluating Active Neuronetics rTMS stimulator and Inactive Neuronetics rTMS stimulator for Depression. Completed, enrolled 12 participants across 1 site.

Detailed Summary

The purpose of this study is to determine the safety and efficacy of rTMS as an alternative treatment to ECT. The study will also provide data for a power analysis to support a larger clinical trial if there is evidence of a clinically relevant treatment effect.

Study Details

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

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedMar 6, 2014
Enrollment StartMar 1, 2014
Primary CompletionDec 1, 2015
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 12.3 years ago

Interventions

Active Neuronetics rTMS stimulatordevice

In the active group, magnetic power output will be delivered to the subject through the coils.

Inactive Neuronetics rTMS stimulatordevice

In the inactive group, no magnetic power output will be delivered to the subject through the coils.