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Transcranial Magnetic Stimulation in Depression

This study has been completed.
Study NCT00018746.   Last updated on June 23, 2005.   Information provided by Department of Veterans Affairs

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Descriptive Information Fields
Brief Title  Transcranial Magnetic Stimulation in Depression
Official Title  Efficacy of Threshold Vs. Subthreshold TMS in the Treatment of Depression
Brief Summary

The study examines efficacy of repetitive transcranial magnetic stimulation in treating severely depressed patients who are medicated.

Detailed Description

Medicated, treatment resistant, depressed patients are randomized to active or sham repetitive transcranial magnetic stimulation (rTMS). Responding patients go into a six months follow-up period.

Study Phase Phase I
Study Type  Interventional
Study Design  Treatment, Randomized, Single Blind, Placebo Control, Crossover Assignment, Efficacy Study
Primary Outcome Measure 
Secondary Outcome Measure 
Condition  Depression
Intervention  Device: repetitive transcranial magnetic stimulation
MEDLINE PMIDs
Links
Recruitment Information Fields
Recruitment Status  Completed
Enrollment 
Start Date  July 1999
Completion Date July 2001
Eligibility Criteria 

severe treatment-resistant depression

Gender Both
Ages 18 Years and older
Accepts Healthy Volunteers No
Contacts ††
Location Countries  United States
Administrative Information Fields
NCT ID  NCT00018746
Organization ID MHBS-037-98S
Secondary IDs ††
Study Sponsor  Department of Veterans Affairs
Collaborators ††
Investigators 
Investigator:     Ralph Hoffman        
Investigator:     Dan Oren        
Information Provided By Department of Veterans Affairs
Verification Date December 2004
First Received Date  July 3, 2001
Last Updated Date June 23, 2005

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.




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