Viewing Study NCT01909232



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Last Modification Date: 2024-10-26 @ 11:10 AM
Study NCT ID: NCT01909232
Status: COMPLETED
Last Update Posted: 2016-07-28
First Post: 2013-07-22

Brief Title: A Clinical Trial for the Treatment of Depression With Repetitive Transcranial Magnetic Stimulation rTMS
Sponsor: Cervel Neurotech Inc
Organization: Cervel Neurotech Inc

Study Overview

Official Title: A Prospective Double-Blind Randomized Parallel-Group Sham-Controlled Feasibility Trial of Multi-Coil Repetitive Transcranial Magnetic Stimulation rTMS for the Treatment of Major Depressive Disorder
Status: COMPLETED
Status Verified Date: 2016-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to determine whether the Cervel Neurotech rTMS device is safe and effective in the treatment of depression in people who do not get better with antidepressant medications or cannot take antidepressant medications
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None